The invention relates to a breast care device that addresses breast complications associated with breastfeeding which may include thrush or yeast infection, cracked nipples, breast pain, sore nipples, engorged breasts, clogged ducts, milk blisters, bites among others.
Many mothers experience different types of breast pain and discomfort during postpartum lactation. These conditions may include thrush or yeast infection, cracked nipples, breast pain, sore nipples, engorged breasts, clogged ducts, bites, or milk blisters. These complications can make breastfeeding an uncomfortable experience and even cause a mother to stop breastfeeding altogether.
Breastfeeding is a crucial part of a baby's development. Breast milk has been proven to protect babies from allergies and eczema, as well as reduce risk of viruses, urinary tract infections, and respiratory infections. Research has also suggested that babies who are breastfed have higher IQ scores later in their life in comparison to children who were not breastfed. In addition to benefitting the baby, breastfeeding is also beneficial for moms. A stronger bond is created between the mom and baby because of the skin-to-skin contact during the process. Also, breastfeeding helps lower the risk of breast and ovarian cancer and can help a mother in losing pregnancy weight. Although there are many benefits for breastfeeding, moms are still very likely to stop due to breastfeeding complications or pains.
To deal with these complications such as cracked nipples, thrush, bites, milk blisters among others, one helpful approach is for nursing mothers to treat the breast with a therapeutic solution such as saline solution after breastfeeding. Although the saline solution is helpful in treating breastfeeding pains, it can be difficult for the mother to apply the liquid to the breast.
In addition, current products treating breastfeeding complications use thermal therapy by providing heating or cooling to the breast but do not simultaneously provide medicated treatment or other therapy.
The disclosed device is a breast care device that addresses breast complications associated with breastfeeding which includes thrush or yeast infection, cracked nipples, breast pain, sore nipples, engorged breasts, clogged ducts among others. The breast care device can be used independently or together with other treatment alternatives depending on the need of the use. The breast care device may be a complete bra, a strapless bra, or an insert to place into the user's bra. The disclosed device may have a system that can fit breasts of 95% female anthropometric data.
In some embodiments, the breast care device features a system to hold fluid or medication on the breast. The system may include a reservoir chamber that may be made out of a range of synthetic materials such as silicone, polypropylene, urethanes, and rubbers. ‘Reservoir chamber’ and ‘dome-like’ are synonyms with reservoir chamber used in embodiments where fluid is present and dome-like, describing the shape of the geometry, used when fluid is not present. This reservoir chamber may be able to contain fluid such as a therapeutic fluid inside against the breast. A breast care device may comprise an inlet port for receiving the therapeutic fluid and an outlet port to drain the therapeutic fluid. A therapeutic fluid may be a medication.
The reservoir chamber of an exemplary breast care device may include a seal to place and hold on to the breast. The seal will also prevent any fluid or medication from leaking out of the breast care device. The seal may be around the circumference of the reservoir chamber. The seal may be a plurality of passive seals that can hold the reservoir chamber to the breast. Passive seals may be aided with the use of adhesives to the body. The seal may also be an O-ring type design. The seal may be a vacuum seal that can include a syringe or a tube for creating negative pressure in order to improve the seal or fit to the body.
An exemplary breast care device may have an inlet port that can be used to introduce a therapeutic fluid into the reservoir chamber. The system may feature an inlet port that can introduce a therapeutic fluid through the use of a syringe. The system may feature a drain. The drain may be manual and the user will have the ability to empty the reservoir chamber themselves by opening the drain and closing it when needing to refill said reservoir chamber again. The drain may be automatic and empty the reservoir chamber out after a specific amount of time in order to decrease fluid contact with the breast. The automatic drain may drain the used therapeutic fluid to a compartment in the bottom portion of the reservoir chamber that acts as a second reservoir. The system may feature a medicated disposable insert of any shape that is placed inside the reservoir chamber. The disposable insert may be made out of foam. The disposable insert may be a medicated foam. The disposable insert may be a soaked gel pad. The disposable insert may be a pad soaked in therapeutic solution. The disposable insert may be a fluid pouch to release therapeutic fluid into the reservoir chamber and the reservoir chamber may have actuation feature to allow the user to release the fluid. The disposable insert or reservoir chamber may have channels to allow slow release of therapeutic fluid. The disposable insert may feature an adhesive to stick to the reservoir chamber.
According to another embodiment, the breast care device may feature said reservoir chamber as described in the previous embodiment that has therapeutic light elements attached to the inside part that may be facing the breast. The light elements may be light emitting diode light bulbs. The light elements may shine light on the breast for the purpose of phototherapy. Phototherapy treatment may be used to heal and relieve pain due to breastfeeding. The light elements may be powered by a battery pack. The light elements may be powered by wall power. The breast care device, similar to the previous embodiment, may also include said seal to the body that can be passive or a vacuum seal.
In another embodiment, the breast care device may feature said reservoir chamber as described in previous embodiments with an electrical grid at the device-breast interface. The electrical grid may be made of mesh fabric and may be used on its own without the reservoir chamber and placed on top of the breast. The electrified components may be powered by battery pack. The electrified components may be powered by an electrical outlet and power cord coupling the breast care device thereto. The breast care device, similar to the previous embodiments, may also include said seal to the body that may be passive or a vacuum seal. The electrified components may include a vibration mechanism. The electrified components may alternatively include a rolling mechanism for the purpose of massage.
The breast care device may have components of a smart system that enables a user to operate it using a phone or a remote control.
The breast care device may work in conjunction with a system defined as a “complete” bra, where the breast care device is sandwiched between the breast and the cup of the complete bra. For this usage, ‘complete’ can be described as an article of fabric clothing meant to cover and possibly offer support to the breast. A complete bra also can be described as having two straps over the shoulder that hold the fabric to the user.
Another embodiment of a complete bra would include a bra with one strap or without any straps.
The breast care device may have components including an ultrasound mechanism for the purpose of imaging or therapy. Such a component would be coupled to the device through either the reservoir chamber or attachment to the dome-like surface and may utilize a fluid-medium (within the reservoir chamber) for transmission of sound waves.
The summary of the invention is provided as a general introduction to some of the embodiments of the invention and is not intended to be limiting. Additional example embodiments including variations and alternative configurations of the invention are provided herein
The accompanying drawings are included to provide a further understanding of the invention and are incorporated in and constitute a part of this specification, illustrate embodiments of the invention, and together with the description serve to explain the principles of the invention.
Corresponding reference characters indicate corresponding parts throughout the several views of the figures. The figures represent an illustration of some of the embodiments of the present invention and are not to be construed as limiting the scope of the invention in any manner. Further, the figures are not necessarily to scale, some features may be exaggerated to show details of particular components. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a representative basis for teaching one skilled in the art to variously employ the present invention.
As used herein, the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having” or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Also, use of “a” or “an” are employed to describe elements and components described herein. This is done merely for convenience and to give a general sense of the scope of the invention. This description should be read to include one or at least one and the singular also includes the plural unless it is obvious that it is meant otherwise.
Certain exemplary embodiments of the present invention are described herein and are illustrated in the accompanying figures. The embodiments described are only for purposes of illustrating the present invention and should not be interpreted as limiting the scope of the invention. Other embodiments of the invention, and certain modifications, combinations and improvements of the described embodiments, will occur to those skilled in the art and all such alternate embodiments, combinations, modifications, improvements are within the scope of the present invention.
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This application claims the benefit of U.S. Provisional Patent Application Ser. No. 62/940,051, filed Nov. 25, 2019.
Number | Date | Country | |
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62940051 | Nov 2019 | US |