US20070270886A1 - Apparatus and method for treating gastroesophageal reflux disease - Google Patents

Abstract

A minimally invasive surgical procedure is disclosed which includes the steps forming a fold of tissue, extending one or more needles through the fold of tissue, deploying a tissue fastener from an interior lumen of each of the needles, and retracting each of the needles from the fold of tissue such that the tissue fasteners remain deployed in the fold of tissue.

Description

• This application is a continuation of application Ser. No. 10/314,722, filed Dec. 9, 2002, which claims priority from provisional application Ser. No. 60/342,540 filed Dec. 20, 2001, the entire contents of which are incorporated herein by reference.
BACKGROUND OF THE INVENTION
• 1. Field of the Invention
• The subject invention is directed to a minimally invasive surgical procedure, and more particularly, to an endoscopic surgical procedure for treating gastroesophageal reflux disease, and apparatus for performing the procedure.
• 2. Background of the Related Art
• Gastroesophageal reflux disease (GERD) is one of the most common upper-gastrointestinal disorders in the western world, with a prevalence of approximately 360 cases per 100,000 population per year. Approximately 25% of individuals with GERD will eventually have recurrent, progressive disease and are candidates to undergo anti-reflux surgical procedures for effective long term therapy.
• GERD is a condition in which acids surge upward from the stomach into the esophagus. Backflow of acid into the esophagus makes it raw, red and inflamed, producing the condition known as esophagitis; it also causes the painful, burning sensation behind the breastbone known as heartburn. Backflow or reflux of acid can occur when the sphincter or band muscle at the lower end of the esophagus fails to stay closed. This sphincter is called the lower esophageal sphincter (LES). The LES acts as a valve to the stomach, remaining closed until the action of swallowing forces the valve open to allow food to pass from the esophagus to the stomach. Normally the valve closes immediately after swallowing to prevent stomach contents from surging upward. When the LES fails to provide that closure, stomach acids reflux back into the esophagus, causing heartburn.
• The general approach for corrective surgery involves creating a new valve or tightening the existing valve. This procedure is known as “fundoplication” and is used to prevent the back flow of stomach acids into the esophagus. Various fundoplication procedures have been developed to correct GERD and are known as Nissen fundoplication, Belsey Mark IV repair, Hill repair and Dor repair. Each surgical procedure has its own unique attributes; however, each requires an invasive surgical procedure, whereby the individual must endure trauma to the thoracic cavity. The individual remains hospitalized after the procedure for about six to ten days.
• The Nissen fundoplication technique involves enveloping the lower esophagus with the gastric fundus by suturing the anterior and posterior fundal folds about the esophagus. Modifications of this procedure include narrowing of the esophageal hiatus posterior to the esophagus, anchoring of the fundoplication to the preaortic fascia and surgical division of the vegus nerve. The degree of the fundal wrap can be modified to incompletely encircle the esophageal tube to avoid gas float syndrome and has also been modified to include a loose wrap. Similarly, the Belsey Mark IV repair, Hill repair and Dor repair are directed to modifications for encirclement of the esophageal tube by fascia.
• Complications of these fundoplication procedures include the inability to belch or vomit, dysphagia, gastric ulcer, impaired gastric emptying and slippage of the repair that may foil the best surgical results. Therefore, the fundoplication procedures have been modified to adjust the length and tension of the wrap, include or exclude esophageal muscle in the sutures and leaving the vagus nerves in or out of the encirclement.
• A relatively new fundoplication technique is known as Nissen fundoplication laparoscopy. In contrast to the traditional Nissen fundoplication procedure, which requires a 6 to 10 inch incision and a 6 to 10 day hospital stay with up to 8 weeks of recovery at home, the laparoscopy technique is performed through small openings about the abdominal cavity and most patients tend to leave the hospital in two days and can return to work and other activities within a week or two. Despite the benefits of less invasive laparoscopic fundoplication procedures, there is still a need for a minimally invasive corrective treatment for GERD that can be performed on an out-patient basis.
SUMMARY OF THE INVENTION
• The subject invention is directed to a new and useful minimally invasive surgical procedure for treating Gastroesophageal reflux disease by reducing the diameter of the esophagus proximate to the lower esophageal sphincter, and to an endoscopic surgical apparatus for performing the procedure. The method includes the steps of forming a fold of esophageal tissue proximate to the lower esophageal sphincter, and extending at least one needle through the fold of esophageal tissue. Each of the needles has an interior lumen containing a tissue fastener. The method further includes the steps of ejecting a distal portion of the tissue fastener from the interior lumen of each needle such that the distal portion of each tissue fastener is disposed against a distal surface of the fold of esophageal tissue, and retracting each needle from the fold of esophageal tissue such that a proximal portion of each tissue fastener is deployed from the interior lumen of each needle and is disposed against a proximal surface of the fold of esophageal tissue.
• The method further comprises the step of providing an endoscopic device having a an interior lumen for supporting the needles in a manner that permits the reciprocal movement thereof, and a tissue reception cavity for receiving the fold of esophageal tissue. The method includes guiding the endoscopic device through the esophagus to a location wherein the tissue reception cavity is disposed proximate to the lower esophageal sphincter. Thus, the step of forming the fold of esophageal tissue includes the step of drawing esophageal tissue into the tissue reception cavity of the endoscopic device. This may be accomplished using suction or with a tissue grasping device.
• Preferably, a tissue fastener of shape memory alloy or a similar bio-compatible material having memory characteristics is provided within the interior lumen of each needle in a generally elongate orientation. The step of ejecting a tissue fastener from the interior lumen of a needle includes permitting the distal portion of the tissue fastener to move to a normally unstressed condition (at body temperature) wherein the distal portion of the tissue fastener is in a curved or coiled orientation. The step of retracing the needle from the fold of esophageal tissue includes permitting the proximal portion of the tissue fastener to move to a normally unstressed condition (at body temperature) wherein the proximal portion of the tissue fastener is in a curved or coiled orientation. It is envisioned that the needles may be extended through the fold of esophageal tissue simultaneously or in seriatim. Similarly, the tissue fasteners may be ejected from the needles simultaneously or in seriatim. After the fasteners have been ejected from the needles, the fold of esophageal tissue is released from the tissue reception cavity, and the endoscopic device is withdrawn from the esophagus.
• The subject invention is further directed to an endoscopic surgical apparatus for performing the method summarized above. The apparatus includes an elongated tubular body having opposed proximal and distal end portions and an interior lumen extending therethrough. An endoscope may be housed within the interior lumen of the tubular body. Preferably, one or more needles are disposed within the elongated tubular body and are mounted for reciprocal movement therein between a retracted position and a protracted position. Depending upon the configuration and orientation of the needles within the tubular body, it is envisioned that the reciprocal movement thereof may be either longitudinal, rotational or helical. Each of the needles has an interior lumen extending therethrough. A tissue fastener is disposed within the interior lumen of each needle. The fasteners are configured for movement between an initially straight position within the interior lumen of a needle and a subsequently coiled or curved position ejected from the interior lumen of a needle.
• A mechanism is provided for effectuating reciprocal movement of the needle within the interior bore of the elongated tubular body, and a mechanism if provided for ejecting the tissue fasteners from the interior lumen of the needles. Preferably, a tissue receiving window is formed within the distal end portion of the elongated tubular body for receiving a fold of esophageal tissue. Thus, the retracted position of the needle is proximal to or, in some instances lateral to the tissue receiving window and the protracted position of the needle is distal of the tissue receiving window.
• These and other aspects of the subject invention and the method of using the same will become more readily apparent to those having ordinary skill in the art from the following detailed description of the invention taken in conjunction with the drawings described hereinbelow.
BRIEF DESCRIPTION OF THE DRAWINGS
• So that those having ordinary skill in the art to which the subject invention appertains will more readily understand how to make and use the surgical apparatus disclosed herein, preferred embodiments thereof will be described in detail hereinbelow with reference to the drawings, wherein:
• FIG. 1 is a perspective view of a surgical apparatus constructed in accordance with a preferred embodiment of the subject invention;
• FIG. 1ais an enlarged localized perspective view, in partial cross-section, of the distal portion of the surgical apparatus ofFIG. 1, with parts separated for ease of illustration, wherein the apparatus includes a plurality of elongated needles mounted for reciprocal longitudinal movement relative to the longitudinal axis of the apparatus;
• FIG. 2 is a perspective view of another surgical apparatus constructed in accordance with a preferred embodiment of the subject invention;
• FIG. 2ais an enlarged localized perspective view of the distal portion of the surgical apparatus ofFIG. 2, with parts separated for ease of illustration, wherein the apparatus includes a plurality of curved needles mounted for reciprocal rotational movement relative to the longitudinal axis of the apparatus;
• FIG. 3 is a perspective view of another surgical apparatus constructed in accordance with a preferred embodiment of the subject invention;
• FIG. 3ais an enlarged localized perspective view of the distal portion of the surgical apparatus ofFIG. 3, with parts separated for ease of illustration, wherein the apparatus includes a plurality of partially helical needles mounted for reciprocal helical movement relative to the longitudinal axis of the apparatus;
• FIG. 4 is a side elevational view of the distal portion of the surgical apparatus ofFIG. 1 illustrating the formation of a fold of esophageal tissue proximate to the lower esophageal sphincter during a treatment procedure;
• FIG. 5 is a side elevational view the distal portion of the surgical apparatus ofFIG. 1 illustrating the extension of a needle through the fold of esophageal tissue, wherein the interior lumen of the needle contains a tissue fastener;
• FIG. 6 is a side elevational view the distal portion of the surgical apparatus ofFIG. 1 illustrating the ejection of a distal portion of the tissue fastener from the interior lumen of the needle such that the distal portion of the tissue fastener is disposed against a distal surface of the fold of esophageal tissue;
• FIG. 6ais an enlarged localized view of the needle shown inFIG. 6 illustrating the ejection of the fastener from the interior lumen of the needle by the needle pusher;
• FIG. 7 is a side elevational view of the distal portion of the surgical apparatus ofFIG. 1 illustrating the retraction of the needle from the fold of esophageal tissue such that a proximal portion of tissue fastener is deployed from the interior lumen of the needle and is disposed against a proximal surface of the fold of esophageal tissue; and
• FIG. 7ais an enlarged localized view of the needle shown inFIG. 7 illustrating the retraction of the needle from the fold of tissue.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
• Referring now to the drawings wherein like reference numerals identify similar structural features of the apparatus disclosed herein, there is illustrated inFIG. 1 an endoscopic surgical apparatus constructed in accordance with a preferred embodiment of the subject invention and designated generally byreference numeral10.
• Referring toFIG. 1 in conjunction withFIG. 1a, endoscopicsurgical apparatus10 includes an elongated flexibletubular body12 having opposed proximal anddistal end portions14,16 and aninterior lumen18 extending therethrough. Elongatedflexible needles20 with tapered leading edges are disposed within the elongatedtubular body12 and are mounted for reciprocal longitudinal movement therein between a retracted position and a protracted position. More particularly, the elongated needles20 are supported in circumferentially spaced relationship withintubular body12 by aneedle block25.Needle block25 is mounted at the distal end of atubular drive shaft27 which is adapted for reciprocal axial movement withintubular body12.
• Eachelongated needle20 has aninterior lumen22 extending therethrough. Atissue fastener24 formed of a shape memory metal alloy, such as a nickel-titanium alloy, is disposed within the interior lumen of eachneedle20. Thetissue fastener24 is configured for movement between an initially straight position within the interior lumen of the elongated needle and a subsequently coiled position ejected from the interior lumen of the elongated needle. In the straight position, and in the coiled position,opposed end portions24a,24bof thefastener24 have a generally curved configuration. InFIG. 2a, theend portion24aoffastener24 is shown in the coiled position, while theopposed end portion24bis shown in a transitional state between the initially straight position and the subsequently coiled or curved position.
• Anelongated push rod26 extends through theinterior lumen22 of eachelongated needle20 for ejecting at least a portion of thetissue fastener24 from theinterior lumen22 of theelongated needle20. Eachpush rod26 is supported in circumferentially spaced relationship by apush rod block30. Pushrod block30 is mounted at the distal end of atubular drive shaft29 which is mounted coaxial withdrive shaft27. Driveshaft29 is adapted and configured for reciprocal axial motion withintubular body12.
• As best seen inFIG. 1,surgical apparatus10 further includes anactuation mechanism35 operatively associated with aproximal portion14 of theelongate body12.Actuation mechanism35 is adapted and configured to effectuate reciprocal longitudinal movement of thedrive shaft27 associated withneedle block25 and thedrive shaft29 associated withpush rod block30. It is envisioned thatactuation mechanism35 can take the form of a mechanical actuator, a pneumatic actuator, a hydraulic actuator or an electrical actuator which transmits force to thedrive shafts27,29 through conventional mechanisms, such as cooperative linkages, gear trains or combinations thereof. It is also envisioned that the fasteners can be fired in a proximal direction.
• Surgical apparatus10 further includes a generally U-shaped or concavetissue receiving window32 formed within the distal end portion of the elongatedtubular body12. In the retracted position, the elongated needles20 are proximal of thetissue receiving window32 and in the protracted position, the elongated needles22 travel to a position that is distal to thetissue receiving window32.
• As illustrated inFIG. 1a, as an option, thesurgical apparatus10 of the subject invention could be provided with anangioplasty balloon40 that would be accommodated within anelongated lateral lumen42. It is envisioned thatangioplasty balloon40 could be extended from the distal end oftubular body12 and used as a dilator to increase the esophageal diameter prior to placement of thefasteners24.
• Referring toFIGS. 2 and 2a, there is illustrated anothersurgical apparatus110 constructed in accordance with a preferred embodiment of the subject invention that includes anelongated body112 having opposed proximal anddistal end portions114 and116, and aninterior lumen118 extending therethrough. Thedistal end portion116 has atissue receiving window132 formed therein and theproximal portion114 has an actuator handle135 operatively associated therewith.
• As best seen inFIG. 2a,surgical apparatus110 includes a plurality ofcurved needles120 each supporting asurgical fasteners124 in theinterior lumen122 thereof. Thecurved needles120 are supported in axially spaced relationship on aneedle block125 that is mounted for reciprocal rotational movement withinbody portion112. A plurality ofcurved push rods126 are supported on apush rod block130adjacent needle block125. Eachpush rod126 is configured to eject at least a portion of atissue fastener124 from theinterior lumen122 of aneedle120 upon actuation of handle135. Those skilled in the art will readily appreciate that conventional mechanisms such as drive screws or drive shafts may be employed to transmit rotational motion from actuation handle135 to needle block125 and pushrod block130.
• Referring toFIGS. 3 and 3a, there is illustrated anothersurgical apparatus210 constructed in accordance with a preferred embodiment of the subject invention that includes anelongated body212 having opposed proximal anddistal end portions214 and216, and aninterior lumen218. Atissue receiving window232 is formed in thedistal end portion216 and anactuator handle235 is operatively associated with theproximal potion214. As best seen inFIG. 3a,surgical apparatus210 differs fromsurgical apparatus110 in that it includes a plurality of partiallyhelical needles220 that are mounted for reciprocal helical movement withinbody portion212 relative to the longitudinal axis ofbody portion212.
• While not shown inFIG. 3a, a surgical fastener formed from shape memory alloy is supported with theinterior lumen222 of eachneedle220 and is configured for deployment in the manner described above with respect toapparatus110. Those skilled in the art will readily appreciate that conventional mechanisms such as drive screws or drive shafts may be employed to transmit helical motion from actuation handle235 to the needle block and push rod block operatively associated withcurved needles220.
• The subject invention is also directed to a method of treating gastroesophageal reflux disease using a surgical apparatus constructed in accordance a preferred embodiment of the subject invention, such as, for example,surgical apparatus10. Initially, during a surgical procedure, theelongated body12 ofsurgical apparatus10 is extended through the esophagus such thattissue receiving window32 is positioned in a location that is proximate to the esophageal sphincter. Next, as shown inFIG. 4, a fold of esophageal tissue is drawn into thetissue receiving window32. This is preferably done under visual observation using theflexible endoscope50 extended through theinterior lumen18 ofbody12, and is preferably accomplished by suction or using a tissue grasping device such astissue grasper45.
• Thereafter, one ormore needles20 are extended through the fold of esophageal tissue, as shown inFIG. 5. At such a time, thedistal portion24aof thetissue fastener24 in eachneedle20 is ejected from theinterior lumen22 of eachneedle20 bypush rod26 such that thedistal portion24aof eachtissue fastener24 is disposed against a distal surface of the fold of esophageal tissue in a curved condition, as shown inFIGS. 6 and 6a. Then, as shown inFIGS. 7 and 7a, needles20 are retracted from the fold of esophageal tissue such that theproximal portion24bof eachtissue fastener24 is deployed from theinterior lumen22 ofneedle20 and is disposed against a proximal surface of the fold of esophageal tissue.
• In instances wherein more than one needle is employed, the needles may be extended through the fold of esophageal tissue either simultaneously or in seriatim by staging the needles at different positions relative to one another. Similarly, the tissue fasteners may be ejected from the needles simultaneously or in seriatim by staging the push rods at different positions relative to one another. After the needles have been retracted, the fold of esophageal tissue is released from the tissue reception cavity.
• Once thefasteners24 have been deployed, the fold of tissue with which they are associated will undergo repetitive movement during peristalsis. Since the ends of the fasteners are curved and flexible, they will advantageously comply with the fold of tissue as it moves. This flexibility also accommodates belching and vomiting. Furthermore, the flexible configuration of the fasteners facilitates the easy removal thereof from the fold of tissue should it become necessary to reverse the procedure. This may be done with a grasping device, such as that which is illustrated inFIG. 4.
• Preferably, the steps of the subject invention are performed under vision using an endoscope which may be provided integral withsurgical device10. Alternatively, the treatment method of the subject invention may be performed using either ultrasound, fluoroscopy or magnetic resonance imaging.
• It is also envisioned and well within the scope of the subject invention that thesurgical apparatus10 and the method of using the same can be employed to reduce the volume of a patients stomach. In such a procedure, gastric tissue would be fastened using the apparatus of the subject invention. Since the ends of the fasteners utilized in this procedure are curved and flexible, they will comply or unfurl with the fold of tissue as the stomach expands with the intake of food.
• Although the apparatus and method of the subject invention have been described with respect to preferred embodiments, those skilled in the art will readily appreciate that changes and modifications may be made thereto without departing from the spirit and scope of the present invention as defined by the appended claims.

Claims (18)

1. A method of treating gastroesophageal reflux disease comprising the steps of:

a) forming a fold of esophageal tissue proximate to the lower esophageal sphincter;

b) extending a needle through the fold of esophageal tissue, the needle having an interior lumen containing a tissue fastener;

c) ejecting a distal portion of the tissue fastener from the interior lumen of the needle such that the distal portion of the tissue fastener is disposed against a distal surface of the fold of esophageal tissue; and

d) retracting the needle from the fold of esophageal tissue such that a proximal portion of tissue fastener is deployed from the interior lumen of the needle and is disposed against a proximal surface of the fold of esophageal tissue.

2. A method according toclaim 1, further comprising the step of providing an endoscopic device having a tissue reception cavity formed in a distal end portion thereof and the step of forming the fold of esophageal tissue includes the step of drawing esophageal tissue into the tissue reception cavity of the endoscopic device.

3. A method according toclaim 2, wherein the step drawing esophageal tissue into the tissue reception cavity of the endoscopic device is performed under suction.

4. A method according toclaim 2, wherein the step of drawing esophageal tissue into the tissue reception cavity of the endoscopic device is performed with a tissue grasping device.

5. A method according toclaim 2, further comprising the step of guiding the endoscopic device through the esophagus to a location wherein the tissue reception cavity is disposed proximate to the lower esophageal sphincter.

6. A method according toclaim 2, further comprising the step of providing the needle within an interior lumen of the endoscopic device.

7. A method according toclaim 6, further comprising the step of providing the tissue fastener within the interior lumen of the needle in an initial condition wherein the fastener is in a generally elongate orientation and wherein the step of ejecting the staple from the interior lumen of the needle includes permitting the distal portion of the tissue fastener to move to a normal condition wherein the distal portion of the tissue fastener is in a curved orientation.

8. A method according toclaim 7, wherein the step of retracting the needle from the fold of esophageal tissue includes permitting the proximal portion of the tissue fastener to move to a normal condition wherein the proximal portion of the tissue fastener is in a curved orientation.

9. A method according toclaim 1, further comprising the step of providing an endoscope for performing the steps of the method under vision.

10. A method according toclaim 9, wherein the endoscope is provided as an integral part of the endoscopic device.

11. A method according toclaim 1, further comprising the steps of extending at least one other needle containing a tissue fastener through the fold of esophageal tissue, and deploying the distal and proximal portions of the tissue fastener against respective surfaces of the fold of esophageal tissue.

12. A method according toclaim 11, wherein the needles are extended through the fold of esophageal tissue simultaneously and the tissue fasteners are ejected from the needles simultaneously.

13. A method according toclaim 11, wherein the needles are extended through the fold of esophageal tissue in seriatim and the tissue fasteners are ejected from the needles in seriatim.

14. A method of applying a surgical fastener to gastro-esophageal tissue comprising the steps of:

a) forming a fold of gastro-esophageal tissue;

b) extending at least one needle through the fold of tissue, the at least one needle having an interior lumen containing a tissue fastener formed from shape memory metal disposed in an initial condition;

c) ejecting a distal portion of the tissue fastener from the interior lumen of the needle such that the distal portion of the tissue fastener moves to a normally curved condition against a distal surface of the fold of tissue; and

d) retracting the needle from the fold of tissue such that a proximal portion of tissue fastener is deployed from the interior lumen of the needle and moves to a normally curved condition against a proximal surface of the fold of tissue.

15. A method according toclaim 14, further comprising the step of providing an endoscopic device having a tissue reception cavity formed in a distal end portion thereof and the step of forming the fold of gastro-esophageal tissue includes the step of drawing tissue into the tissue reception cavity of the endoscopic device.

16. A method according toclaim 15, wherein the step of drawing tissue into the tissue reception cavity of the endoscopic device is performed under suction.

17. A method according toclaim 15, wherein the step of drawing tissue into the tissue reception cavity of the endoscopic device is performed with a tissue grasping device.

18-29. (canceled)

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