Device and method for treatment of gastroesophageal reflux disease

Information

  • Patent Grant
  • 6604004
  • Patent Number
    6,604,004
  • Date Filed
    Thursday, October 4, 2001
    23 years ago
  • Date Issued
    Tuesday, August 5, 2003
    21 years ago
Abstract
A lower esophageal sphincter tightening device for treating gastroesophageal reflux disease which includes an insertion device, an energy source, and an energy transmitting device. The insertion device, by insertion through a body opening, positions the energy transmitting device in the proximity of the lower esophageal sphincter. The energy source generates and transmits energy via the insertion device to the energy transmitting device which directs the transmitted energy onto the lower esophageal sphincter which is comprised largely of collagen. The energy sources transmits energy at a level sufficient to cause heating of the sphincter's collagen resulting in a shrinkage of the collagen and a tightening of the sphincter.
Description




BACKGROUND OF THE INVENTION




The invention pertains to the treatment of gastroesophageal reflux disease (GERD).




GERD is a major health problem in the United States and worldwide. It affects tens of millions of people and costs billions of dollars to treat. GERD is the reflux of gastric contents from a stomach into a lower area of an esophagus. The gastric contents include acid secreted by the stomach which causes discomfort and eventual damage to an inner lining of the esophagus if left untreated.




The gastric contents are normally prevented from entering the esophagus by a lower esophageal sphincter (LES) mechanism. The LES is a physiologic, non-anatomic area involving the lower 3 centimeters of the esophagus and like other smooth muscle sphincters in the body, anal or urinary, it is tonically contracted to prevent reflux. A healthy LES opens for a brief period of several; seconds in response to swallowing to allow the passage of food. It then quickly regains its tone when the food has passed.




GERD occurs when the sphincter mechanism of the LES fails to work properly. Generally, GERD takes one of three forms: (i) complete weakness of the sphincter musculature in response to a hiatal hernia or an intrinsic weakness that occurs commonly resulting in free reflux, which is poorly understood; (ii) partial weakness of the sphincter that allows reflux when stressed such as a Valsalva maneuver, or (iii) transient or sudden inappropriate relaxation of an otherwise normally toned sphincter.




Treatment of a weakened or inappropriately relaxing sphincter can be either medical or surgical. Known medical treatments include measures or medications that attempt to decrease acid secretion, increase gastric emptying or strengthen the LES. However, the medications are expensive and the measures typically have to be continued on a life long basis.




A more permanent treatment method for GERD can be performed surgically. Surgical methods attempt to strengthen the LES by incising the stomach and wrapping a portion of the stomach around the lower section of the esophagus. This technique is known as a fundoplication. However, surgical treatment requires longer post treatment care, increased pain and recovery time, as well as the associated risks with any surgical procedure.




The latest developments for treating GERD have attempted to provide a minimally invasive procedure to strengthen the lower esophageal area One such treatment is disclosed by C. P. Swain et al.,


Knot Tying At Flexible Endoscopy


, Gastrointestinal Endoscopy, 1994; 40:722-29, that calls for endoscopic sewing in the lower esophageal area. However the sewn portion of the esophagus in the Swain technique may relax again requiring further or alternate forms of treatment Another technique disclosed by Donahue injects noxious, scarring substances into the lower esophageal area to create a fibrous reaction P. E. Donahue, et. al.,


Endoscopic Ultrasonography Verifies Effect On Endoscopic Treatment Of Reflux In Dogs And Man


, Surgical Endoscopy, 1993;7:524-28. However, the Donahue technique may require numerous and repeated injections.




The esophagus and LES are composed of three tissue layers; a mucosa or inner layer, a submucosa or middle layer, and a muscle or an outer layer. The submucosa layer is largely composed of collagen. It is well-known that heating of collagen tissue within an appropriate temperature range results in a tightening or shrinkage of the collagen tissue. However, there exists no known device or technique for strengthening the LES by shrinkage of collagen tissue as a means to treat GERD.




SUMMARY OF THE INVENTION




The invention discloses a device and method to prevent gastroesophageal reflux or GERD. The device comprises an insertion device, an energy source, and an energy transmitting device. The insertion device has a proximal end connected to the energy source and a distal end connected to the energy transmitting device. The energy source generates and transmits energy to the energy transmitting device through the insertion device. The energy transmitting device then radiates and directs the transmitted energy onto a target area. The insertion device positions the energy transmitting device in the proximity of a lower esophageal sphincter, such that the sphincter tissue becomes the target area of the energy transmitting device.




The energy source then generates and transmits energy to the energy transmitting device which radiates the energy onto the sphincter tissue. The sphincter tissue absorbs the radiated energy which generates heat within the sphincter tissue. The sphincter tissue is largely comprised of collagen which exhibits shrinkage when heated.




The energy source generates and transmits energy at a level sufficient to cause heating of the sphincter tissue to a temperature of between 50° C. and 70° C. (preferably between 63° C. and 65° C. within a time period of between about 1 microsecond and 1 minute. Heating the sphincter tissue within the appropriate range achieves sufficient collagen shrinkage to tighten the lower esophageal sphincter and prevent reflux.











BRIEF DESCRIPTION OF THE DRAWINGS





FIG. 1

is a perspective view of a lower esophageal sphincter tightening device of the present invention.





FIG. 2

is a cutaway diagram of an esophagus.





FIG. 3

is a perspective view of a second embodiment of the lower esophageal sphincter tightening device of the present invention.





FIG. 4

is a perspective view of a third embodiment of the lower esophageal sphincter tightening device of the present invention.











DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS





FIG. 1

, a preferred embodiment of a lower esophageal sphincter (LES) tightening device


10


is shown in use. The LES tightening device


10


comprises an insertion device


12


, an energy source


14


and an energy transmitting device


16


. As shown in

FIG. 1

, the LES tightening device


10


could also include an inflation device


18


and a balloon


20


.




In a preferred embodiment, the insertion device


12


is an endoscope as shown in

FIGS. 1

,


3


and


4


. However, workers skilled in the art will recognize that a catheter or other similar device could also be used. As shown in

FIG. 1

, the insertion device


12


has a proximal end


22


and a distal end


24


. Additionally, the insertion device


12


could include an eye piece


26


, a light source


28


and a control means


30


. A series of ports


32


provide access from the proximal end


22


to the distal end


24


through lumens located within the interior of the insertion device


12


along its longitudinal access.




The energy source


14


is located at the proximal end


22


of the insertion device


12


. The energy source


14


generates and transmits energy to the energy transmitting device


16


located at the distal end


24


of the insertion device


12


. The energy source


14


is connected to the energy transmitting device


16


by a transmission line


34


which passes through a manifold


36


. Within the manifold


36


, the transmission line


34


becomes part of a catheter


38


that is fed through one of the ports


32


at the proximal end


22


. The catheter


38


then passes down one of the interior lumens of the insertion device


12


and is connected to the energy transmitting device


16


at the distal end


24


.




In a preferred embodiment, the insertion device


12


enters a body opening


40


and passes down an esophagus


42


until the distal end


24


is in the proximity of a lower esophageal sphincter


44


. The control means


30


aid in positioning the distal end


24


of the insertion device


12


. Observation through eye piece


26


insures proper placement of the distal end


24


. Observation is enabled by the light source


28


which illuminates the area surrounding the distal end


24


by light transmitted through an optical cable


45


which passes through one of the ports


32


and down another interior lumen. The optical cable


45


is preferably a fiber optic bundle.




The energy transmitting device


16


radiates and directs energy received through the catheter


38


from the energy source


14


onto a target area. The distal end


24


of the insertion device


12


is therefore located such that the target area of the energy transmitting device


16


is directed at tissue comprising the lower esophageal sphincter


44


. Once the energy transmitting device


16


is properly positioned, the energy source


14


can transmit energy it has generated to the energy transmitting device


16


through the catheter


38


.




The transmitted energy is then radiated and directed by the energy transmitting device


16


onto the lower esophageal sphincter


44


tissue. The lower esophageal sphincter


44


tissue absorbs the energy resulting in the generation of heat within the tissue due to thermal conduction. The lower esophageal sphincter


44


tissue is comprised largely of collagen which will exhibit shrinkage characteristics over an appropriate time temperature relationship prior to being damaged or destroyed.




The appropriate time period to satisfy the time temperature relationship is dependent upon the temperature of the treated tissue, which in turn is dependent upon the level of energy generated in the energy source


14


and radiated by the energy transmitting device


16


. The desired tissue temperature in the target area is between 50° C. and 70° C., with a preferred level between 63° C. and 65° C. This temperature increase can be achieved within a period of time between one microsecond and one minute dependent upon the amount and type of energy generated within the energy source


14


. In a preferred embodiment, the energy source


14


generates radiant energy (e.g. RF or microwave electromagnetic energy) which is transmitted by a transmission line


34


(such as a coaxial cable) that is then contained within the catheter


38


and connects to the energy transmitting device


16


. The energy transmitting device


16


is preferably an antenna or a directional antenna.




The LES tightening device


10


can additionally include the inflation device


18


and the balloon


20


. Once the energy transmitting device


16


is properly positioned, the balloon


20


is located at the distal end


24


of the insertion device


12


and encapsulates the energy transmitting device


16


as shown in FIG.


1


. The inflation device


18


, located at the proximal end


22


, inflates or deflates the balloon


20


via a conduit


48


. The conduit


48


connects the inflation device


18


to the balloon


20


by passing through the manifold.


36


, wherein the conduit


48


becomes part of the catheter


38


. Air, fluid or gel could be used by the inflation device


18


to inflate the balloon


20


. The size of the balloon


20


can be adjusted to maintain proper placement of the energy transmitting device


16


in relation to the lower esophageal sphincter


44


tissue and/or control the amount of collagen shrinkage and therefore control the amount of sphincter tightening.




In a preferred embodiment, the balloon


20


can be either a noncompliant balloon or a compliant balloon. The size of a compliant balloon can be controlled by observation through the eye piece


26


, injection of a radiopaque fluid such as fluorochrome into the balloon


20


and viewing on a fluoroscope, or monitoring the pressure of the balloon


20


.





FIG. 2

is a cutaway schematic view (not to scale) of the tissue comprising the lower esophageal sphincter


44


. The tissue is comprised of three layers; a mucosa


48


inner layer, a submucosa


50


middle layer and a muscle


52


outer layer. In a preferred embodiment, collagen tissue in the submucosa


50


is targeted for shrinkage. In addition, a cooling means to prevent damage to the mucosa


48


may be incorporated into the LES tightening device


10


. This can be accomplished by cooling or cycling through cooled air, liquid, or gel to inflate the balloon


20


. The cooled material dissipates the heat generated by absorption of the radiated energy from the energy transmitting device


16


. This maintains a safe temperature level in the mucosa


46


(which is less than about 50° C. or preferably less than 45° C.) The type and amount of cooled material used to inflate the balloon


20


is dependent on the amount and type of energy generated within the energy source


14


.





FIG. 3

shows a second embodiment of the LES tightening device


10


. Reference numerals identical to those employed in connection with

FIG. 1

indicate identical elements, and reference numerals followed by a suffix indicate modified but similar elements. In this preferred embodiment, the energy transmitting device


16


A is attached to the outer surface of the balloon


20


A to direct energy at the lower esophageal sphincter


44


tissue. As previously described, once the distal end


24


of the insertion device


12


properly positions the energy transmitting device


16


A over the lower esophageal sphincter


44


tissue, the balloon


20


A can be inflated and the energy source


14


can transmit energy to the energy transmitting device


16


A for radiation onto the lower esophageal sphincter


44


tissue. Again, a coolant can be used to inflate the balloon


20


A to prevent damage to the mucosa


48


while achieving collagen shrinkage in the submucosa


50


resulting in the tightening of the lower esophageal sphincter


44


.




A third alternative embodiment to the present invention is depicted in FIG.


4


. Again, reference numerals identical to those employed in connection with

FIG. 1

indicate identical elements, and reference numerals followed by a suffix indicate modified but similar elements. In this embodiment, the balloon


20


B is enlarged to protrude into a stomach


46


and anchor or retain the energy transmitting device


16


B in proper position with respect to the lower esophageal sphincter


44


tissue. In this embodiment, the insertion device


12


positions the energy transmitting device


16


B such that the target area comprises the lower esophageal sphincter


44


tissue. Once in place, the balloon


20


B is enlarged by injection of a suitable material which retains the position of the energy transmitting device


16


B relative to the lower esophageal sphincter


44


. This assures the energy radiated by the energy transmitting device


16


B is absorbed by the lower esophageal sphincter


44


. Again, the material injected into the balloon


20


B for inflation can be cooled to a sufficient level to offset and dissipate any heat build-up in the mucosa


48


and thereby enable the generation of heat and consequent shrinkage of collagen in the submucosa


50


.




Although the present invention has been described with reference to treatment of GERD by toning the muscular LES sphincter, workers skilled in the art will recognize that this device and method could be used to shrink or tone other sphincters located in the body to overcome other medical ailments caused by the loss of sphincter muscle tone. For example, the device and method can be used on the urinary or anal sphincter to overcome incontinence.




Furthermore, workers skilled in the art will also recognize that changes may be made in form and detail without departing from the spirit and scope of the invention. For example, the energy source can generate energy of various wavelengths within the electromagnetic spectrum including but not limited to laser, RF, or microwave energy. Alternatively, the energy source can generate ultrasonic energy to generate heat in the targeted tissue area. The insertion device can be an endoscope, catheter or similar type of device. Depending on the form and wavelength of the energy being used, the energy transmitting device may be an antenna, an ultrasonic transducer, a fiber optic bundle, or an electrical resistance heater. Furthermore, a directional antenna can be used to limit and control the amount of energy directed at specific locations within the targeted tissue.




With the present invention, tissue within the lower esophageal sphincter can be toned or tightened to treat gastroesophageal reflux disease on an outpatient basis with a safe, simple procedure with decreased aftercare, treatment and pain.



Claims
  • 1. A device for toning or tightening a gastroesophageal sphincter within a body, the device comprising:a. an insertion device having a proximal end and a distal end, wherein the insertion device is configured for insertion into a body opening and comprising expandable structure for positioning an energy transmitting device proximate a target area in a tower esophageal sphincter; b. an energy source located at the proximal end of the insertion device; c. an energy transmitting device located at the distal end of the insertion device; and d. observation and control pieces proximate the proximal end to aid in proper positioning of the distal end; and wherein the energy transmitting device is communicably connected to the energy source through the insertion device, and wherein the energy transmitting device comprises a plurality of antennae positioned upon outer or inner surfaces of the expandable structure for directing energy generated by the energy source to an area of tissue making up the targeted tissue area of the sphincter to heat the targeted tissue area to a temperature greater than about 50° C. in the targeted tissue area of the gastroesophageal sphincter.
  • 2. The device of claim 1, further comprising a fiber optic cable at the distal end of the insertion device communicably connected to an eye piece at the proximal end of the device.
  • 3. The device of claim 1, wherein the structure for positioning comprises an expandable structure adapted to prevent dispersion of heat generated in the targeted tissue by compressing the targeted tissue area.
  • 4. The device of claim 1, wherein said energy transmitting device comprises a structure suitable for causing collagen shrinkage for tightening the lower esophageal sphincter.
  • 5. The device of claim 1, wherein the energy transmitting device comprises antennae for directing energy generated by the energy source to an area of tissue making up the targeted tissue area of the sphincter to heat the targeted tissue area to a temperature of between 63° and 65° C. in the targeted tissue area.
  • 6. The device of claim 1, wherein the energy source generates electromagnetic energy.
  • 7. The device of claim 1, wherein the insertion device comprises an endoscope.
  • 8. The device of claim 1, and further including means for cooling surface tissue of the sphincter to prevent surface tissue damage while the energy transmitting device radiates energy.
  • 9. The device of claim 8, wherein the means for cooling dissipates heat generated in the sphincter surface tissue to maintain a temperature below about 50° C. in the surface tissue.
  • 10. The device of claim 1, wherein the expandable structure comprises an inflatable balloon.
  • 11. The device of claim 10, wherein the inflatable balloon is located with the energy transmitting device proximate the distal end of the insertion device and is communicably connected through the insertion device to an inflation device located at the proximal end of the insertion device.
  • 12. The device of claim 1, wherein the energy transmitting device comprises a portion which extends generally radially away from the insertion device.
Parent Case Info

This application is a continuation of Ser. No. 09/475,580 filed Dec. 30, 1999, U.S. Pat. No. 6,321,121 which is a continuation of Ser. No. 08/749,723 filed Nov. 15, 1996, U.S. Pat. No. 6,073,052.

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Continuations (2)
Number Date Country
Parent 09/475580 Dec 1999 US
Child 09/971315 US
Parent 08/749723 Nov 1996 US
Child 09/475580 US