Patent Application
20230355424
When an ostomy appliance or wafer is changed, care must be taken to properly clean and prepare the stoma and surrounding area before a new appliance or wafer can be positioned for use. It may take several minutes for a patient or caregiver to clean and prepare the skin during which time the stoma may be exposed. While the stoma is exposed, leakage from the stoma may occur and can lead to patient discomfort or result in increased efforts to clean and prepare the surrounding area.
A stoma covering device according to various aspects of the present technology may comprise an open ended body having an internal receiving area configured to receive and be positioned over the stoma to temporarily cover the stoma during the changing process of an ostomy device or wafer. The open ended body may be configured to be held in place in a hands-free manner and without the aid of adhesives, straps, or other mechanical devices. A resilient body may be attached to the open ended body and be used to create a low pressure region within the internal receiving area prior to the stoma covering device being positioned over the stoma.
A more complete understanding of the present technology may be derived by referring to the detailed description and claims when considered in connection with the following illustrative figures. In the following figures, like reference numbers refer to similar elements and steps throughout the figures.
Elements and steps in the figures are illustrated for simplicity and clarity and have not necessarily been rendered according to any particular sequence. For example, steps that may be performed concurrently or in a different order are illustrated in the figures to help to improve understanding of embodiments of the present technology.
The present technology may be described in terms of functional block components and various processing steps. Such functional blocks may be realized by any number of components configured to perform the specified functions and achieve the various results. For example, the present technology may employ various types of materials and connection devices for coupling components together. In addition, the present technology may be practiced in conjunction with any number of physical activities, and the system described is merely one exemplary application for the technology. Methods and apparatus for a covering device for a stoma according to various aspects of the present technology may operate in conjunction with any suitable materials such as rubber, nylon, plastic, polymers, or other natural or synthetic materials.
Referring to
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With particular reference now to
The mid-body section 114 may also comprise any suitable length (distance along the longitudinal axis 300) to provide a sufficient interior volume to the interior receiving portion 106 so that the stoma can be enclosed comfortably. For example, the mid-body section 114 may comprise a length of between about 10 mm and about 30 mm.
The cap portion 102 may comprise any suitable material capable of repeated use. For example, the cap portion 102 may be formed of a rigid or semi-rigid plastic or polymer that is capable of being cleaned or sanitized for reuse. Alternatively, the cap portion 102 may comprise a material intended for single use that may be less rigid and less capable of being cleaned such as paper, cardboard, or the like while still being able to withstand a pressure differential between the interior receiving portion 106 and the ambient environment. The material may also be selected based on its density to help reduce the overall weight of the cap portion 102. For example, a lighter weight cap portion 102 may be require a lower pressure differential between the interior receiving portion 106 and the ambient environment to hold the stoma covering device 100 in place during use.
Referring now to
The compressible ball portion 602 may comprise a round body having an interior volume that is open to the exterior of the compressible ball portion 602 through a passage 606 extending through the insertion end 604. The insertion end 604 may be configured to be inserted into the second open end 110 of the cap portion so that the interior volume of the compressible ball portion 602 is in fluid communication with the interior receiving portion 106 of the cap portion 102.
In operation, during a changing procedure, a user may remove an existing ostomy appliance and replace it with a new ostomy appliance. After the existing ostomy appliance is removed from the stoma, the user may place the first open end 108 of the cap portion 102 over the stoma so that the outer peripheral edge encircles the base of the stoma and the stoma is received into the interior receiving portion 106. Prior to the outer peripheral edge being fully positioned against the user's skin, the user may compress the resilient body member 104 thereby reducing the interior volume inside of the resilient body member 104. Air contained within the interior volume may exit through the first open end 108 of the cap portion 102 via the passage 606 adjacent to the second open end 110.
Then, the outer peripheral edge of the first open end 108 may be seated firmly against the user's skin and the resilient body member 104 is allowed to move from a compressed state to an uncompressed state. As the resilient body member 104 expands to its fully uncompressed state, air is drawn into the interior volume from the interior receiving portion 106 via the passage 606 causing the pressure within the interior volume and the interior receiving portion 106 to decrease below the pressure of the ambient environment surrounding the stoma covering device 100.
The reduction in pressure within the interior receiving portion 106 causes the outer peripheral edge of the first open end 108 to be drawn, or otherwise held, against the user's skin creating a seal so that no air can pass into the interior receiving portion 106. The lower relative pressure inside the interior receiving portion 106 then acts to hold the stoma covering device 100 in place over the stoma allowing the user to have both hands free to clean and prepare the area around the stoma and be able to contain any leakage from the stoma to the interior receiving portion 106. For example, the user may be able to remove an existing ostomy wafer, clean and condition the skin around the stoma, place a new ostomy wafer, without having to hold the stoma covering device 100 in place. When the user is ready to place a new ostomy device over the stoma, the user may remove the stoma covering device 100 by separating the outer peripheral edge of the first open end 108 from the user's skin and thereby allowing the pressure within the interior receiving portion 106 and interior volume of the resilient body 104 to equalize with the ambient conditions. A further benefit is that any leaked material from the stoma may be collected into the interior receiving portion 106 so it may be discarded. The stoma covering device 100 may then be cleaned and reused.
The particular implementations shown and described are illustrative of the technology and its best mode and are not intended to otherwise limit the scope of the present technology in any way. Indeed, for the sake of brevity, conventional manufacturing, connection, preparation, and other functional aspects of the system may not be described in detail. Although embodiments of the present technology have been described with reference to use with a stoma, the technology should not be viewed as being limited in that respect.
The description and figures are to be regarded in an illustrative manner, rather than a restrictive one and all such modifications are intended to be included within the scope of the present technology. Accordingly, the scope of the technology should be determined by the generic embodiments described and their legal equivalents rather than by merely the specific examples described above. For example, the components and/or elements recited in any apparatus embodiment may be assembled or otherwise operationally configured in a variety of permutations to produce substantially the same result as the present technology and are accordingly not limited to the specific configuration recited in the specific examples.
As used herein, the terms “comprises,” “comprising,” or any variation thereof, are intended to reference a non-exclusive inclusion, such that a process, method, article, composition or apparatus that comprises a list of elements does not include only those elements recited but may also include other elements not expressly listed or inherent to such process, method, article, composition or apparatus. Other combinations and/or modifications of the above-described structures, arrangements, applications, proportions, elements, materials or components used in the practice of the present technology, in addition to those not specifically recited, may be varied or otherwise particularly adapted to specific environments, manufacturing specifications, design parameters or other operating requirements without departing from the general principles of the same. Any terms of degree such as “substantially,” “about,” and “approximate” as used herein mean a reasonable amount of deviation of the modified term such that the end result is not significantly changed. For example, these terms can be construed as including a deviation of at least ±5% of the modified term if this deviation would not negate the meaning of the word it modifies.
The present technology has been described above with reference to exemplary embodiments. However, changes and modifications may be made to the exemplary embodiments without departing from the scope of the present technology. These and other changes or modifications are intended to be included within the scope of the present technology, as expressed in the following claims.
