This invention relates to percutaneous endoscopic gastrostomy (PEG) tubes, and in particular, to a PEG tube having an improved internal bumper that reduces the chance of the tube accidentally being pulled out or dislodged.
PEG tubes are placed in patients who are not able to ingest food down the esophagus and provide feed to the patient directly into the stomach, preventing malnutrition. These are usually trauma, stroke, head or neck cancer patients going through chemotherapy, and young patients who have trouble swallowing. Today there are two main styles of device being used commercially with two different internal bumper designs and insertion methods. There are mushroom internal bumpers inserted using the pull method and balloon internal bumpers inserted using the push method and inflated inside the stomach.
The tubes are prone to being pulled out or dislodged from the patient, leading to infection and additional surgeries. Approximately 216,000 PEG tubes were placed in the year 2000, and that number will grow with growth of the elderly population. The PEG tube can be placed in a patient in an operating room under either local or general anesthesia or in an outpatient setting. The two methods that are commonly used for placing the PEG tube are the pull method and the push method, with the pull method being the most common method used for PEG tube insertion. The pull method is illustrated in
A PEG tube can also be placed using the push method where the tube and internal bumper are pushed through an incision site in the stomach of the patient. This method commonly uses balloon bumpers instead of the mushroom bumpers used in the pull method.
Regardless of the insertion method used, the tubes are designed to be pulled out as early as one month after being inserted, but unruly patients or nurses who are moving patients can pull out the tubes prematurely. The hole in the patient's stomach that hardens around the tube (similar to an earring hole) is referred to as a tract. Typically, tracts would take about one week to mature and harden, but can take up to three weeks in these patients because they were previously malnourished causing slower wound healing. If a tube is removed once the tract is formed after three to four weeks, a Foley catheter can be used to keep the tract open. If the tract has not formed yet, a new tube will be placed in a different location and the old tract will heal in approximately 24-48 hours. Re-insertion of a new tube involves another surgical procedure costing approximately $20,000.
The internal bumper, when pulled too hard against the stomach wall, can migrate into the gastric wall and epithelial layer of the abdominal wall causing buried bumper syndrome (BBS). Many times this disease is not caught until months or years after PEG tube placement. This problem has lessened with new softer bumpers being used, as data has shown that harder plastic bumpers increase the rates of BBS. If this occurs, the tube will have to be removed in surgery and a new tube will be placed in a different spot while the old tract heals. Any pulling on the tube can lead to feed coming in contact with the abdominal wall or skin and can cause infection as the food seeps into the abdominal space. Infection from the feed can cause many different health problems, including death. Statistics show that approximately 7.8% of the patients who receive PEG tubes die from complications. Minor complications, including tube dislodgement, occur in as many as 88% of patients.
A need exists for a PEG tube that prevents or reduces the possibility of dislodgement and therefore prevents or reduces the likelihood of patients having to undergo additional surgeries and additional pain.
Representative embodiment in accordance with the inventive principles and concepts are directed to a PEG tube comprising PEG tubing and an internal bumper. The PEG tubing has a proximal end and a distal end. The internal bumper is disposed on the proximal end of the PEG tubing. The internal bumper is in a first, placed state when the PEG tube is in a feeding position inside of a patient. In the first, placed state, the internal bumper is a substantially solid structure having a preselected shape and a preselected maximum outer diameter or width. Initiation of a removal process converts the internal bumper from the first, placed state to a second, removal state in which the internal bumper is converted into a generally elongated structure that has an outer diameter or width that is smaller than the maximum outer diameter or width when it is in the first, placed state to facilitate withdrawal of the generally elongated structure through a tract in the patient's stomach through which the PEG tubing extends when the PEG tube is in the feeding position.
In accordance with a representative embodiment, initiation of the removal process is performed by actuating a conversion mechanism that cuts a preselected pattern in the internal bumper to thereby convert the internal bumper from the first, placed state to the second, removal state.
In accordance with a representative embodiment, the conversion mechanism comprises a wire or cord having a proximal end, a distal end and a length of wire or cord extending from the proximal end to the distal end of the wire or cord. A portion of wire or cord near the proximal end of the wire or cord is embedded in the material comprising the internal bumper in a preselected pattern. The distal end of the wire or cord extends out of the distal end of the PEG tubing. The wire or cord is actuated by pulling on the distal end of the wire or cord to cause the portion of the wire or cord that is embedded in the material to cut through the material to convert the internal bumper into the generally elongated structure.
These and other features and advantages will become apparent from the following description, drawings and claims.
In accordance with the inventive concepts and principles, a new internal bumper design is provided that prevents, or at least reduces the chances of, unintended dislodgement of the PEG tubes, thereby limiting complications associated therewith. The PEG tube comprises PEG tubing and an internal bumper. The PEG tubing has a proximal end and a distal end. The internal bumper is disposed on the proximal end of the PEG tubing. The internal bumper is in a first, placed state when the PEG tube is in a feeding position inside of a patient. In the first, placed state, the internal bumper is a substantially solid structure having a preselected shape and a preselected maximum outer diameter or width. Initiation of a removal process converts the internal bumper from the first, placed state to a second, removal state in which the internal bumper is converted into a generally elongated structure that has an outer diameter or width that is smaller than the maximum outer diameter or width when it is in the first, placed state to facilitate withdrawal of the generally elongated structure through a tract in the patient's stomach through which the PEG tubing extends when the PEG tube is in the feeding position.
In the following detailed description, a few illustrative, or representative, embodiments are described to demonstrate the inventive principles and concepts. For purposes of explanation and not limitation, representative embodiments disclosing specific details are set forth in order to provide a thorough understanding of an embodiment according to the present teachings. However, it will be apparent to one of ordinary skill in the art having the benefit of the present disclosure that other embodiments according to the present teachings that depart from the specific details disclosed herein remain within the scope of the appended claims. Moreover, descriptions of well-known apparatuses and methods may be omitted so as to not obscure the description of the representative embodiments. Such methods and apparatuses are clearly within the scope of the present teachings.
The terminology used herein is for purposes of describing particular embodiments only, and is not intended to be limiting. As used in the specification and appended claims, the terms “a,” “an,” and “the” include both singular and plural referents, unless the context clearly dictates otherwise. Thus, for example, “a device” includes one device and plural devices. Relative terms may be used to describe the various elements' relationships to one another, as illustrated in the accompanying drawings. These relative terms are intended to encompass different orientations of the device and/or elements in addition to the orientation depicted in the drawings. It will be understood that when an element is referred to as being “connected to” or “coupled to” another element, it can be directly connected or coupled, or intervening elements may be present.
Exemplary, or representative, embodiments will now be described with reference to the figures, in which like reference numerals represent like components, elements or features. It should be noted that features, elements or components in the figures are not intended to be drawn to scale, emphasis being placed instead on demonstrating inventive principles and concepts.
In accordance with a representative embodiment, the internal bumper is generally disk-shaped and adapted to be inserted into the patient using an endoscope via the pull method described above with reference to
Currently, known PEG tubes are removed solely by pulling the tube out through the tract in the stomach, which can lead to accidental premature dislodgement and pain to the patient. In accordance with a representative, or illustrative, embodiment, the internal bumper is removed by pulling a cord or wire when the internal bumper needs to be removed. As this cord is pulled, it cuts around the disk-shaped internal bumper in a spiral resulting in a corkscrew-shaped piece of bumper material (e.g., silicone) attached to the end of the tubing. The outer diameter of the corkscrew-shaped piece of bumper material is smaller than the diameter of the tract in the stomach formed by the PEG tube to allow the tube with the corkscrew-shaped piece of bumper material attached to the end of it to be easily pulled through the tract without risking complications, such as BBS, for example.
The tubing 13 of the PEG tune 10 and the internal bumper 11 may be integrally formed of a suitable material, such as, for example, silicone or latex. A suitable process, such as injection molding, for example, may be used to manufacture the PEG tube 10 with the internal bumper 11 integrally formed on the proximal end 13a of the tubing 13. Alternatively, the tubing 13 and the internal bumper 11 may be manufactured as separate parts and subsequently secured to one another by a suitable process and/or material (e.g., glue or other type of adhesive, plastic welding, etc.). The PEG tube 10 is not limited to being made of any particular material or by any particular process, as will be understood by those of skill in the art in view of the description provided herein.
In accordance with this representative embodiment, a thin wire or cord 14 of a suitable material (e.g., medical grade metal that will not degrade inside of the human body), is embedded in the material comprising the internal bumper 11 and arranged in a suitable pattern, which is a spiral pattern in accordance with the representative embodiment shown in
The proximal end 14a (
With reference to
In order to intentionally remove the PEG tuber 10, the person performing the removal process grasps the distal end 14b of the wire or cord 14 extending out of the distal end 13b of the tubing 13 and pulls it. As this wire or cord 14 is pulled, it cuts around the internal bumper 11 in the spiral pattern in which the wire or cord 14 is arranged in the material comprising the internal bumper 11. This act of pulling on the wire or cord 14 causes it to cut through the material comprising the internal bumper 11 at the locations in the material in which the wire or cord 14 is disposed, resulting in a corkscrew-shaped piece of bumper material (e.g., silicone) attached to the end of the tubing 13. The outer diameter of the corkscrew-shaped piece of bumper material is smaller than the diameter of the tract in the stomach formed by the PEG tube to allow the tube with the corkscrew-shaped piece of bumper material attached to the end of it to be easily pulled through the tract without risking complications, such as BBS, for example.
It should be noted that the internal bumper 11 may have shapes other than the shape of a disk, as will be understood by those of skill in the art in view of the description provided herein. The internal bumper is generally a solid structure that has a desired characteristics of flexibility and rigidity that allow the tubing to be handled without accidentally disengaging the bumper. The desired characteristics of flexibility and rigidity can be achieved by selecting a material (e.g., silicone) and process for forming the bumper (e.g., injection molding) that provide a structure that has the desired degrees of flexibility and rigidity. For example, selecting a less flexible silicone, forming a thicker bumper structure and/or treating the silicone with one or more chemicals that change its characteristics through one or more chemical reactions are ways of achieving the desired flexibility and rigidity.
Regardless of the shape and size of the internal bumper or the materials and processes that are used to manufacture, it will have a first, placed state after the PEG tube has been placed in a feeding position inside of the patient via the pull method, and it will have a second, removal state when a person or machine is performing the process of removing the PEG tube. In the first, placed state, the internal bumper is fully deployed and is at its maximum size (e.g., maximum outer diameter or width) against the anterior wall of the stomach. In the second, removal state, the internal bumper has been converted into a generally elongated structure having an outer diameter or width that is smaller than the maximum outer diameter or width to facilitate withdrawal of the generally elongated structure through the tract.
It should be noted that illustrative embodiments have been described herein for the purpose of demonstrating principles and concepts of the invention. As will be understood by persons of skill in the art in view of the description provided herein, many modifications may be made to the embodiments described herein without deviating from the scope of the invention. For example, while the inventive principles and concepts have been described with reference to the internal bumper shown in
The present application is a nonprovisional application that claims the benefit of and priority to the filing date of U.S. provisional application Ser. No. 62/653,176, filed on Apr. 5, 2018 and entitled “CONFORMATION CHANGING PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE,” which is hereby incorporated by reference herein in its entirety.
The invention was made with Government support under Contract/Grant No. R25HD078327 awarded by the National Institutes of Health (NIH) and under Contract/Grant No. 1263941 awarded by the National Science Foundation (NSF). The Government has certain rights in the invention.
Number | Date | Country | |
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62653176 | Apr 2018 | US |