Method and apparatus for modifying the exit orifice of a satiation pouch
View Patent ↗A prosthetic device is described that is positionable within the gastro-esophageal junction region of a patient. The prosthetic device includes a proximal opening and a distal orifice that is adjustable in size prior to and/or following implantation. During use, the prosthetic device is attached to tissue of the gastro-esophageal junction region of the patient, with the device positioned such that food ingested by the patient passes from the esophagus through the proximal opening into the interior of the prosthetic device, and eventually exits the prosthetic device via the distal opening.
1. A method of retarding a flow of food from a patient's esophagus into the stomach comprising the steps of:
transorally introducing into the patient's stomach, a plurality of food-restrictive elements that can be physically adjusted to vary the rate of food flow passing from a proximal opening through the device,
attaching the elements within the patient's stomach adjacent the gastro-esophageal junction such that the flow of food from the esophagus into the stomach is restricted by such elements,
monitoring the flow of food into the stomach, and
in response to said monitoring, transorally accessing the stomach and physically cutting an element to increase the food flow rate into the stomach.
2. The method of claim 1 , wherein said plurality of elements includes an implantable device having a proximal opening and a distal opening, and an attachable/detachable restrictor that serves to retard the flow of food through the device by providing an orifice that is smaller than the proximal and distal openings of the device, said method further comprises, after attaching the device to the patient's stomach:
attaching the restrictor to the distal opening of the device.
3. The method of claim 2 , wherein the implantable device has a circumferential recess, said restrictor has a circumferential rim, and said attaching the restrictor further comprises:
placing the restrictor rim within the device recess.
4. The method of claim 2 , wherein said method includes selecting a restrictor having a desired-size orifice.
5. The method of claim 4 , which further includes evaluating the patient to determine whether a restrictor with a different size orifice would be more efficacious, and if so, removing the originally placed restrictor and replacing it with one having a different size orifice.
6. The method of claim 1 , wherein said plurality of elements form a cage structure.