The present disclosure relates to procedures, such as ostomy procedures, where an opening is surgically created in the body for the discharge of body fluid. Some example procedures include colostomy (artificial opening created in abdominal wall to bypass a damaged part of the colon), ileostomy (piece of ileum is diverted to an artificial opening created in abdominal wall), urostomy (artificial opening creating for the urinary system), esophagostomy (artificial opening created in esophagus, such as the cervical section of the esophagus), gastrostomy (artificial opening created in the stomach), etc. For example, the opening may allow waste to be removed from the body. The surgically created openings may result in a stoma, which may be temporary or permanent. The stoma may be used to allow other portions of the body to rest or heal. These procedures require closing devices (traditionally a clamp or tail clip), which close the stoma in-between catheter or bag insertions and other medical procedures.
The present disclosure provides a new and innovative system, method, and apparatus for a medical plug. In an exemplary aspect of the present disclosure, a medical plug apparatus for use in conjunction with an ostomy procedure includes a cap and a flexible, elongated cylindrical shaft. The cap has a top surface, a bottom surface, and a first thickness. The elongated cylindrical shaft extends orthogonally away from the bottom surface of the cap from a proximal end to a distal end. The first thickness extends from the top surface to the bottom surface at the proximal end of the elongated cylindrical shaft. Additionally, the elongated cylindrical shaft has a smooth external surface, a shaft diameter, and a shaft length. The shaft diameter and the shaft length are adapted to plug a stoma cavity upon inserting the elongated cylindrical shaft into the stoma cavity. The bottom surface of the cap includes a gripping portion, a contact portion, and a shoulder between the gripping portion and the contact portion. The shoulder extends around a periphery of the contact portion. The gripping portion includes a first region, a second region, and a second thickness, which extends from the top surface to the gripping portion at the shoulder. Additionally, the gripping portion extends from the top surface towards the bottom surface. The second thickness is less than the first thickness, and the gripping portion has a gripping diameter such that, upon exerting a pulling force on the first region and the second region of the gripping portion, the elongated cylindrical shaft is directed outwardly away from the patient by the pulling force causing a substantially axial tension force on the elongated cylindrical shaft. The contact portion includes a contact diameter, the contact portion extends from the shoulder across the bottom surface of the cap to the proximal end of the elongated cylindrical shaft. The shoulder includes a third thickness, which extends from the gripping portion at the shoulder to the contact portion and the third thickness is less than the first thickness. The gripping diameter is larger than the contact diameter, and the contact portion is adapted to create a seal with a layer of skin of a patient.
In accordance with another exemplary aspect of the present disclosure, a stoma assembly includes a medical plug and a flexible bandage. The medical plug includes a cap and a flexible, elongated cylindrical shaft. The cap has a top surface, a bottom surface, and a first thickness. The elongated cylindrical shaft extends orthogonally away from the bottom surface of the cap from a proximal end to a distal end. The first thickness extends from the top surface to the bottom surface at the proximal end of the elongated cylindrical shaft. Additionally, the elongated cylindrical shaft has a smooth external surface, a shaft diameter, and a shaft length. The shaft diameter and the shaft length are adapted to plug a stoma cavity upon inserting the elongated cylindrical shaft into the stoma cavity. The bottom surface of the cap includes a gripping portion, a contact portion, and a shoulder between the gripping portion and the contact portion. The shoulder extends around a periphery of the contact portion. The gripping portion includes a first region, a second region, and a second thickness, which extends from the top surface to the gripping portion at the shoulder. Additionally, the gripping portion extends from the top surface towards the bottom surface. The second thickness is less than the first thickness, and the gripping portion has a gripping diameter such that, upon exerting a pulling force on the first region and the second region of the gripping portion, the elongated cylindrical shaft is directed outwardly away from the patient by the pulling force causing a substantially axial tension force on the elongated cylindrical shaft. The contact portion includes a contact diameter, the contact portion extends from the shoulder across the bottom surface of the cap to the proximal end of the elongated cylindrical shaft. The shoulder includes a third thickness, which extends from the gripping portion at the shoulder to the contact portion and the third thickness is less than the first thickness. The gripping diameter is larger than the contact diameter, and the contact portion is adapted to create a seal with a layer of skin of a patient. The flexible bandage has an attachment side and an exterior side. The attachment side includes an adhesive coating and the exterior side is smooth. Additionally, the flexible bandage has a size and shape that is adapted to completely cover the cap of the medical plug. The flexible bandage includes a peripheral portion extending beyond the entire outside edge of the cap. The adhesive coating on the attachment side of the peripheral portion enables the flexible bandage to adhere to the patient and form a barrier between the outside edge of the cap and the outside environment.
In accordance with another exemplary aspect of the present disclosure, a medical plug apparatus for use in conjunction with an ostomy procedure, the medical plug apparatus includes a cap and a flexible, elongated cylindrical shaft. The cap has an outside edge, a top surface and a bottom surface. The cylindrical shaft extends orthogonally away from the bottom surface of the cap from a proximal end to a distal end. The elongated cylindrical shaft has a smooth external surface, a predetermined diameter, and a shaft length. The shaft diameter and the shaft length are adapted to plug a stoma cavity upon inserting the elongated cylindrical shaft into the stoma cavity. The top surface of the cap includes a gripping member, and the gripping member includes a raised protrusion extending along a diameter of the cap. Additionally, the gripping member is adapted to transfer a rotational force in a twisting action to dislodge the medical plug and facilitate removal of the medical plug apparatus such that upon exerting a pulling force on the gripping member, the elongated cylindrical shaft is directed outwardly away from the patient by the pulling force causing a substantially axial tension force on the elongated cylindrical shaft, and the bottom surface is adapted to create a seal with a layer of skin of a patient.
In accordance with another exemplary aspect of the present disclosure, a method includes positioning a flexible, elongated cylindrical shaft of a medical plug over a stoma cavity of a patient, and inserting the elongated cylindrical shaft of the medical plug into the stoma cavity of a patient. The medical plug includes a cap having a top surface, a bottom surface, and a first thickness. The elongated cylindrical shaft extends orthogonally away from the bottom surface of the cap from a proximal end to a distal end. Additionally, the first thickness extends from the top surface to the bottom surface at the proximal end of the elongated cylindrical shaft. The elongated cylindrical shaft has a smooth external surface, a shaft diameter, and a shaft length, where the shaft diameter and the shaft length adapted to plug a stoma cavity upon inserting the elongated cylindrical shaft into the stoma cavity. The bottom surface of the cap includes a gripping portion, a contact portion, and a shoulder between the gripping portion and the contact portion. The shoulder extends around a periphery of the contact portion. Additionally, the method includes positioning the contact portion of the cap into close contact with the patient's skin by applying a downward pressure to the top surface of the cap. The contact portion includes a contact diameter, and the contact portion extends from the shoulder across the bottom surface of the cap to the proximal end of the elongated cylindrical shaft. The shoulder includes a third thickness, which extends from the gripping portion at the shoulder to the contact portion and is less than the first thickness. Additionally, the contact portion is adapted to create a seal with a layer of skin of a patient. The gripping portion includes a first region, a second region, and a second thickness. Further, the gripping portion extends from the top surface towards the bottom surface, and the second thickness extends from the top surface to the gripping portion at the shoulder. The second thickness is less than the first thickness. The method also includes exerting a pulling force on the first region and the second region of the gripping portion, to direct the elongated cylindrical shaft outward and away from the patient. The gripping portion has a gripping diameter such that, upon exerting a pulling force on the first region and the second region of the gripping portion, the elongated cylindrical shaft is directed outwardly away from the patient by the pulling force causing a substantially axial tension force on the elongated cylindrical shaft. The gripping diameter is larger than the contact diameter.
Additional features and advantages of the disclosed system, method, and apparatus are described in, and will be apparent from, the following Detailed Description and the Figures.
Referring to the Figures, embodiments of an enteral feeding and gastric pressure relief/suction device are disclosed. As seen in an exemplary stoma assembly 100 illustrated in
In an example embodiment, the medical plug 101 may be made from a single mold or multiple molds. Additionally, the medical plug 101 may be made from polyurethane, silicone, or the like, which advantageously provide sufficient flexibility, durability, chemical resistant properties, and ease of molding. In another example embodiment, the medical plug 101 may be made from polyurethane. If the medical plug 101 is made from multiple molds, the cap 110 and the elongated cylindrical shaft 120 may be bonded together using adhesive, solvent bonding, radio-frequency (RF) welding and/or any other suitable means of affixing. The cylindrical shaft 120 may be adapted to maintain stoma patency and help prevent stoma stenosis (closing or tightening of the stoma). For example, the cylindrical shaft 120 may have sufficient strength and rigidity to prevent the stoma from tightening or closing.
In an example embodiment, the bottom surface 114 of the cap 110 includes a gripping portion 130. The gripping portion 130 may include a gripping diameter (DG) 150. Additionally, the gripping portion 130 may have a second thickness 140 that extends from the top surface of the cap toward the bottom surface. The second thickness 140 is less than the first thickness 116. In an example embodiment the second thickness 140 may be between 0.03 and 0.15 inches. Additionally, the bottom surface 114 may include a contact portion 160 and a shoulder 170 between the gripping portion 130 and the contact portion 160. In the example with the contact portion 160 and the shoulder 170, the second thickness 140 may extend from the top surface 112 to the gripping portion 130 at the shoulder 170. For example, the shoulder 170 may extend around a periphery 136 (as illustrated in
In an example, the contact portion 160 extends from the shoulder 170 across the bottom surface 114 of the cap 110 to the proximal end 128 of the elongated cylindrical shaft 120. The contact portion 160 may include a contact diameter (DC) 164. Additionally, the shoulder 170 includes a third thickness 162, which extends from the gripping portion 130 at the shoulder 170 to the contact portion 160. In an example, the third thickness 162 is less than the first thickness 116. Additionally, the gripping diameter (DG) 150 is larger than the contact diameter (DC) 164. In an example, the contact portion 160 is adapted to create a seal with a layer of skin of a patient.
As further illustrated in
The elongated cylindrical shaft 120 extends orthogonally away from the bottom surface 114 of the cap 110 from a proximal end 128 to a distal end 127. For example, the distal end 127 of the cylindrical shaft 120 is the end that is first inserted into the stoma cavity 60 of a patient (e.g., the furthest extending end beneath the skin of the patient). In an example embodiment, the distal end 127 of the cylindrical shaft 120 may be rounded to aid in insertion, removal, and to prevent injury or irritation. Additionally, the elongated cylindrical shaft 120 may have a smooth external surface 122 to prevent injury when inserting and removing the medical plug 101 from the patient. For example, a stiff or rough cylindrical shaft 120 may cause serious problems including necrosis, damage to the stoma cavity 60, or cause the patient other irritation and discomfort or injury. The cylindrical shaft 120 includes a shaft diameter (DS) 124 and a shaft length (LS) 126. The shaft diameter (DS) 124 and the shaft length (LS) 126 are adapted to plug a stoma cavity. For example, upon inserting the elongated cylindrical shaft 120 into the stoma cavity 60, the shaft length (LS) 126 is adapted to plug the stoma at a required depth. Additionally, the shaft diameter (DS) 124 is adapted to plug the cavity diameter of the stoma cavity 60. In an example embodiment, the shaft diameter (DS) 124 may range from size 5 French (e.g., 5 FR) to size 18 French (e.g., 18 FR). In other example embodiments, the shaft diameter (DS) 124 may depend on the patient's age, weight, gender, etc. Additionally, the shaft diameter (DS) 124 may depend on the type of medical procedure performed on the patient. Similarly, the shaft length (LS) 126 may depend on the patient's age, weight, gender, etc. In another example embodiment, the shaft length (LS) 126 may depend on the type of medical procedure performed on the patient. The shaft length (LS) 126 may range from 0.5 to 2.5 inches.
The raised protrusion 202 may be rectangular. In another example embodiment, the raised protrusion 202 may have other shapes and geometries. Additionally, the raised protrusion 202 may extend to the outer edge 172 of the cap 110. In other embodiments, the raised protrusion 202 may only partially extend along the top surface 112 of the cap 110. For example, the raised protrusion 202 may be tapered such that it has the largest height (HP) 220 at the center of the cap 110 and has a gradually decreasing height (HP) 220 as it approaches the outside edge 172 of the cap 110. Additionally, the gripping member 130 may included rounded corners (as illustrated in
As illustrated in
In an example embodiment, the images or shapes may be represented in one dimension. In other example embodiments, the images or shapes may be represented in multiple dimensions (e.g., two-dimensions or three-dimensions). The images or shapes may be selected based on age, gender, personal interest, etc. For example, a cap 110 may include the logo of a patient's favorite sports team. Additionally, the cap 110 may include a patient's favorite cartoon character, favorite animal, etc. In other example embodiments, the medical plug apparatus 101 may be colored to provide positive psychological associations with the patient. For example, the medical plug apparatus 101 may be colored red. The medical plug apparatus 101 may include other colorants and additives, such as glitter, or may glow in the dark to encourage use of the medical plug apparatus 101. In an example, the medical plug 101 may include one or more colorants that are adapted to contrast an outside environment, such as the floor, to reduce the likelihood of losing or misplacing the medical plug 101.
Additionally, the flexible bandage 103 may have a size and shape that is adapted to completely cover the cap 110 of the medical plug 101. For example, the flexible bandage 103 includes a peripheral portion 180 extending beyond the entire outside edge 172 of the cap 110. The peripheral portion 180 may sized to ensure that the flexible bandage 103 has enough surface area to form a solid adhesive bond with the patient's skin. In an example embodiment, the adhesive coating 109 on the attachment side 105 of the peripheral portion 180 enables the flexible bandage 103 to adhere to the patient and form a barrier between the outside edge 172 of the cap 110 and the outside environment. The flexible bandage 103 may be opaque. In other example embodiments, the flexible bandage 103 may be clear or colored. For example, as discussed above, the flexible bandage may be colored or include an image that is pleasing to the patient.
The example process 500 may begin with a clinician or patient positioning an elongated cylindrical shaft 120 over a stoma cavity 60 of the patient (block 510). Then, the clinician or patient may insert the elongated cylindrical shaft 120 of the medical plug 101 into the stoma cavity 60 of the patient (block 520). In an example embodiment, the distal end 127 of the cylindrical shaft 120 may be rounded to assist in positioning and inserting the shaft 120 within the stoma cavity 60. Additionally, the cylindrical shaft 120 may include a smooth external surface 120 to reduce injury. The patient or clinician may coat the cylindrical shaft 120 with a lubricant, such as a water soluble lubricant before insertion. Once the cylindrical shaft 120 is inserted, the clinician or patient may position the contact portion 160 of the cap 110 into close contact with the patient's skin (block 530). In an example, the bottom surface 114 and/or the contact portion 160 of the cap is adapted to create a seal with a layer of skin to prevent contaminants from entering the stoma cavity 60. Then, the clinician or patient may position a flexible bandage over the cap 110 of the medical plug 101 (block 540). For example, the clinician or patient may position the flexible bandage 103 such that the medical plug is centered under the bandage 103 (e.g., there is a sufficient peripheral portion 180 around all sides of the medical plug 101). Then, the clinician or patient may press the flexible bandage 103 onto the cap 110 and the patient's skin (block 550). The bandage 103 may include an attachment side 105 with an adhesive coating 109. For example, the adhesive coating may include gelatin, pectin, and carboxy-methycellulose such that it maintains most conditions under the attachment side 105 of the bandage 103. After some time, the patient or clinician may remove the flexible bandage 103 (block 560). Then, the patient or clinician may exert a pulling force 800 on the first region 132 and the second region 134 of the gripping portion 130 to direct the elongated cylindrical shaft 120 outward and away from the patient (block 570). Additionally, the patient or clinician may exert a pulling force on a gripping member 200 or other gripping surfaces 220 on the medical plug 101. In an example, the clinician or patient may twist and/or rotate the cap 110 to dislodge the medical plug 101 through radial force acting perpendicular to the smooth surface 122 of the elongated cylindrical shaft 120. The radial force may interact between the cylindrical shaft 120 and the stoma cavity 60 to loosen the medical plug 101 from the stoma cavity 60.
It should be understood that various changes and modifications to the example embodiments described herein will be apparent to those skilled in the art. Such changes and modifications can be made without departing from the spirit and scope of the present subject matter and without diminishing its intended advantages. It is therefore intended that such changes and modifications be covered by the appended claims. Also, it should be appreciated that the features of the dependent claims may be embodied in the systems, methods, and apparatus of each of the independent claims.
The present application is tile national stage entry of International Patent Application No. PCT/US2017/065559, having a filing date of Dec. 11, 2017, which claims priority to U.S. Provisional Application Ser. No. 62/435,216, filed on Dec. 16, 2016, both of which are incorporated herein in their entirety by reference thereto.
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/US2017/065559 | 12/11/2017 | WO |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2018/111755 | 6/21/2018 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
2243529 | Grossman et al. | May 1941 | A |
4836214 | Sramek | Jun 1989 | A |
4921481 | Danis et al. | May 1990 | A |
4941869 | D'Amico | Jul 1990 | A |
5045052 | Sans | Sep 1991 | A |
5108430 | Ravo | Apr 1992 | A |
5125897 | Quinn | Jun 1992 | A |
6036673 | Quinn | Mar 2000 | A |
6334064 | Fiddian-Green | Dec 2001 | B1 |
6357447 | Swanson et al. | Mar 2002 | B1 |
6451883 | Chen | Sep 2002 | B1 |
6485476 | von Dyck | Nov 2002 | B1 |
6540724 | Harris | Apr 2003 | B1 |
7780639 | Van Lue | Aug 2010 | B2 |
7818155 | Stuebe et al. | Oct 2010 | B2 |
8147486 | Honour et al. | Apr 2012 | B2 |
8388586 | Weig | Mar 2013 | B2 |
8613702 | Feer et al. | Dec 2013 | B2 |
8777912 | Nishtala | Jul 2014 | B2 |
8986230 | Nishtaia | Mar 2015 | B2 |
9179971 | Kirschenman | Nov 2015 | B2 |
9226878 | Elia et al. | Jan 2016 | B2 |
9295395 | Elia et al. | Mar 2016 | B2 |
9345612 | Hanuka | May 2016 | B2 |
9517157 | Hanuka | Dec 2016 | B2 |
9532739 | Bennett-Guerrero | Jan 2017 | B2 |
9610227 | Elia | Apr 2017 | B2 |
9642779 | Elia et al. | May 2017 | B2 |
9713579 | Elia et al. | Jul 2017 | B2 |
9883964 | Hanuka | Feb 2018 | B2 |
10071234 | Koelper | Sep 2018 | B2 |
10441455 | Eggert | Oct 2019 | B2 |
10524953 | Hanuka | Jan 2020 | B2 |
10786652 | Doshi | Sep 2020 | B2 |
10966907 | Puckett | Apr 2021 | B2 |
11224732 | Nordquist | Jan 2022 | B2 |
11395757 | Eggert | Jul 2022 | B2 |
20030040768 | Greene | Feb 2003 | A1 |
20030204174 | Cisko, Jr. | Oct 2003 | A1 |
20060224131 | Calvert | Oct 2006 | A1 |
20070142780 | Van Lue | Jun 2007 | A1 |
20080097179 | Russo | Apr 2008 | A1 |
20080167607 | Pfeiffer et al. | Jul 2008 | A1 |
20080249467 | Burnett et al. | Oct 2008 | A1 |
20100069859 | Weig | Mar 2010 | A1 |
20100280489 | Nishtala | Nov 2010 | A1 |
20110282311 | Nishtala | Nov 2011 | A1 |
20120016256 | Mabary et al. | Jan 2012 | A1 |
20120277619 | Starkebaum et al. | Nov 2012 | A1 |
20130225946 | Feer et al. | Aug 2013 | A1 |
20130304008 | Hanuka | Nov 2013 | A1 |
20150094675 | Kyvik | Apr 2015 | A1 |
20160113843 | Elia et al. | Apr 2016 | A1 |
20160129223 | Kirschenman | May 2016 | A1 |
20160143815 | Koelper | May 2016 | A1 |
20160256665 | Doshi | Sep 2016 | A1 |
20160287428 | Eggert | Oct 2016 | A1 |
20160325088 | Nordquist | Nov 2016 | A1 |
20160331298 | Burnett et al. | Nov 2016 | A1 |
20170071502 | Bennett-Guerrero | Mar 2017 | A1 |
20170202750 | Elia | Jul 2017 | A1 |
20180078195 | Sutaria et al. | Mar 2018 | A1 |
20180161249 | Elia et al. | Jun 2018 | A1 |
20180289536 | Burnett | Oct 2018 | A1 |
Number | Date | Country |
---|---|---|
0 369 923 | May 1990 | EP |
2529922 | Mar 2016 | GB |
2001514051 | Sep 2001 | JP |
1099958 | Jun 1984 | SU |
WO 9007311 | Jul 1990 | WO |
WO 9217150 | Oct 1992 | WO |
WO 9911302 | Mar 1999 | WO |
Entry |
---|
International Search Report and Written Opinion for PCT/US2017/065559, dated Mar. 6, 2018, 16 pages . |
Number | Date | Country | |
---|---|---|---|
20190380861 A1 | Dec 2019 | US |
Number | Date | Country | |
---|---|---|---|
62435216 | Dec 2016 | US |