CESAREAN SECTION INCISION SHELL
20220000675 · 2022-01-06
Inventors
- Katherine Anne Bourdillon (Leeds, GB)
- Rush Lloyd Bartlett, II (Austin, TX, US)
- Kirsten Georgia Granger (Kirsten, GB)
Cpc classification
A61F13/0243
HUMAN NECESSITIES
A61F2013/0028
HUMAN NECESSITIES
International classification
Abstract
An example device for facilitating healing of a Cesarian section incision on a patient can include: a base configured to attach to skin of the patient, at least partially surrounding the Cesarian section incision; and a dome coupled with the base and extending over the Cesarian section incision, wherein the dome is configured to resist collapse when the device is worn under clothing.
Claims
1. A device for facilitating healing of a Cesarian section incision on a patient, the device comprising: a base configured to attach to skin of the patient, at least partially surrounding the Cesarian section incision; and a dome coupled with the base and extending over the Cesarian section incision, wherein the dome is configured to resist collapse when the device is worn under clothing.
2. The device of claim 1, wherein the base is made of soft, flexible silicone.
3. The device of claim 1, wherein the base surrounds the dome and extends approximately about 5.0 mm outward from the dome.
4. The device of claim 1, wherein a skin contact surface of the base comprises a texture.
5. The device of claim 1, wherein a skin contact surface of the base comprises an adhesive.
6. The device of claim 1, wherein the dome is made of a material selected from the group consisting of silicone, polyurethane, polyether, PVC and PVA.
7. The device of claim 1, wherein the dome comprises multiple apertures to facilitate air circulation through the dome.
8. The device of claim 7, wherein the multiple apertures comprise: a first set of apertures near a first end of the dome; and a second set of apertures near a second end of the dome.
9. The device of claim 1, wherein the dome is integrated into a textile postpartum compression product.
10. The device of claim 9, wherein the textile postpartum compression product is a support band.
11. The device of claim 10, wherein the support band is sized to fit around a torso of the patient.
12. The device of claim 1, wherein the base and the dome include a curve.
13. The device of claim 1, wherein the dome comprises one or more compression members.
14. A method of facilitating healing of a Cesarian section incision on a patient, the method comprising: applying a shell dressing over the Cesarian section incision, the shell dressing comprising: a base configured to attach to skin of the patient, at least partially surrounding the Cesarian section incision; and a dome coupled with the base and extending over the Cesarian section incision, wherein the dome is configured to resist collapse when worn under clothing, and wherein when the shell dressing is applied to the patient, neither the base nor the dome contacts the Cesarian section incision.
15. The method of claim 14, further comprising promoting air circulation through the dome of the shell dressing by providing the dome with multiple apertures.
16. The method of claim 15, wherein the multiple apertures comprise: a first set of apertures near a first end of the dome; and a second set of apertures near a second end of the dome.
17. The method of claim 14, further comprising applying a therapeutic agent to the Cesarian section incision before applying the shell dressing.
18. The method of claim 14, wherein the dome is integrated into a textile postpartum compression product.
19. The method of claim 18, wherein the textile postpartum compression product is a support band.
20. The method of claim 19, wherein the support band is sized to fit around a torso of the patient.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0006]
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[0009]
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DETAILED DESCRIPTION
[0014] The various concepts introduced above and discussed in greater detail below may be implemented in any of numerous ways, as the described concepts are not limited to any manner of implementation. Examples of specific implementations and applications are provided primarily for illustrative purposes.
[0015] The C-section dressing or shell described herein protects the incision area of a woman's abdomen post-Cesarian section, without directly touching the incision. This allows the incision to heal, relieving postpartum abdominal pain and discomfort, while reducing the risk of bacterial contamination and subsequent infection.
[0016]
[0017] The flat base 101 may be made of soft, flexible silicone, for example, which lies flat on the skin, ensuring good contact with the skin around the incision. In one embodiment, the flat base 101 extends approximately about 5.0 mm outward from the dome 102. In other embodiments, the flat base 101 may extend from about 0.1 mm to about 30 mm from the dome 102 of the shell 100. The skin-contact surface of the soft, flexible silicone of the flat base 101 may have a sufficient amount of inherent tack (or “stickiness”) to make the flat base 101 stay in position on, and adhere to, the skin, without using any additional adhesive agents. In one embodiment, the tacky silicone is uniform across the entire skin contact surface of the flat base 101. In some embodiments, the tack/stickiness of the skin-contact surface of the flat base 101 may be optimized by giving the surface a texture, pattern or dot-coating on either the entire surface or on sections. The tack is such that the flat base 101 can be moved and replaced on the skin while maintaining adhesive functionality. Alternatively or additionally, the flat base 101 may be coated with a secondary adhesive to facilitate attachment to the skin. Examples of such adhesives include, but are not limited to, acrylic, hydrocolloid, hydrogel, Polyurethane, and rubber adhesives. In some embodiments, such an adhesive may be coated onto a woven or non-woven material that is about 1-15% wider than the flat base 101 and is used as a secondary dressing to secure the C-section shell 100 in place.
[0018] In some embodiments, the semi-rigid dome 102 is also made of silicone. Alternatively, the semi-rigid dome 102 may be made of any number of semi-rigid polymers, such as but not limited to Polyurethane, polyether, PVC and PVA. Whatever material(s) is used, the semi-rigid dome 102 is constructed to resist compression by clothing and other materials and forces that might be applied to it during the activities of daily living.
[0019] Referring now to
[0020] Referring now to
[0021] Referring now to
[0022] In a further embodiment shown in
[0023] Similarly, a pouch with or without an internal opening to create airspace against the skin when the shell is inserted could be used within the garment such that the pouch was opened and the shell was inserted and then the shell was closed to enable securement where the shell rests inside a pouch and gives the pocket of the pouch a ridged or semi-ridged shape while the garment closure, wrap, or other mechanism such as Velcro or snaps are used to secure the top outer portion of the garment closure to the pouch. In other such embodiments the compartment or position where a c-section structural support shell is used within a garment could be made such that there could also be room for a hot/cold pack element. This hot or cold pack element could enable the shell or the surrounding area to provide cooling or heating to that area.
[0024] Similarly in another such embodiment the garment could be made to be reversible such that the hot or cold pack element in the pocket, groove, slot, or other mechanism for positioning of an element of hot or cold pack or shell could be made into the position on the back instead of on the c-section shell area. See
[0025] In any of the above-described embodiments, the C-section shell may be combined with a topical application of one or more therapeutic substances for example in the following therapeutic uses: treatment of pain, healing of tissue, anti-itch, postpartum depression, reduction of infection risk, swelling and or bleeding reduction, and other therapeutic benefits as prescribed and delivered to the site of care by the device construction disclosed herein. These therapeutically active ingredients may include, but are not limited to, anti-inflammatory or pain relieving drugs (ibuprofen or NSAIDs, lidocaine, benzocaine, acetocaine, tetracaine, prilocaine, menthol, morphine, oxycodone, acetaminophen, ethanol, cannabinoids/cannabis, hemp oils, paracetamol, codeine, Nefopam, Flupirtine, Ziconotide), anticonvulsant drugs (carbamazepine, gabapentin, pregabalin, gabapentinoids, and others including those used to treat neuropathic pain), vasoconstrictors (pseudoephedrine, epinephrine, Phenylephrine), anti-depressants (tricyclic antidepressants, lithium etc.), vitamins and their derivatives (vitamin D2 and D3, vitamin C, ascorbyl palmitate, ascorbic acid, vitamin E, argan oil), antimicrobials (Silver, iodine, chlorhexidine, PHMB, Quaternary Ammonium compounds, anti-fungal agents), other anti-inflammatory agents (capsaicin, resveratrol), wound healing promotors (hydrogel, Carboxymethyl cellulose, Collagen, Collagen-ORC) and any other desired material that has a therapeutic effect that may be achieved through local delivery of the therapeutically active material to the surface of the incision site.
[0026] This is believed to be a complete and accurate description of embodiments and aspects of the invention. Alternative embodiments are contemplated within the scope of the invention, however, and the above description is intended for exemplary purposes and not to limit the scope of the invention as described, for example, in the following claims.