143 results about "Breast augmentation" patented technology

Methods of treating patients for conditions such as breast augmentation, soft tissue defects, and urinary incontinence, are described. The methods include removing adipose tissue from a patient, processing a portion of the adipose tissue to obtain a substantially isolated population of regenerative cells, mixing the regenerative cells with another portion of adipose tissue to form a composition, and administering the composition to the patient from which the adipose tissue was removed.

A biodegradable, flexible covering for a breast implant is provided which comprises one or more biodegradable polymer layers dimensioned and shaped to cover at least a portion of the breast implant. The implant can be inserted into an opening of the covering immediately prior to surgery, but alternate configurations and times of insertion are contemplated as well as open or sheet type devices. The coverings can optionally contain one or more drugs for delivery at the surgical site, particularly for treating or preventing infection, pain, inflammation, capsular contracture, scarring or other complications associated with breast augmentation or breast reconstruction.

Methods of treating patients for conditions such as breast augmentation, soft tissue defects, and urinary incontinence, are described. The methods include removing adipose tissue from a patient, processing a portion of the adipose tissue to obtain a substantially isolated population of regenerative cells, mixing the regenerative cells with another portion of adipose tissue to form a composition, and administering the composition to the patient from which the adipose tissue was removed.

A stem-cell-seeded porous scaffold implant and delivery systems for treating or augmenting a breast tissue defect in a patient.

A breast template for delivering stem cell formulation to a breast defect of a patient for treating or augmenting a breast tissue defect comprising a flexible band with at least one throughput hole for guiding an injecting needle to penetrate into the breast of the patient, wherein the flexible band is configured to be placed intimately against a surface of the breast.

The present invention provides muscle-derived progenitor cells that show long-term survival following transplantation into body tissues and which can augment soft tissue following introduction (e.g. via injection, transplantation, or implantation) into a site of soft tissue. Also provided are methods of isolating muscle-derived progenitor cells, and methods of genetically modifying the cells for gene transfer therapy. The invention further provides methods of using compositions comprising muscle-derived progenitor cells for the augmentation and bulking of mammalian, including human, soft tissues in the treatment of various cosmetic or functional conditions, including malformation, injury, weakness, disease, or dysfunction. In particular, the present invention provides treatments and amelioration for dermatological conditions, gastroesophageal reflux, vesico-ureteral reflux, urinary incontinence, fecal incontinence, heart failure, and myocardial infarction.

A three-dimensional fabric structure in a form of a pocket for use in a breast reconstruction surgical procedure such as single-stage or two-stage breast reconstruction. The silk scaffold employs a knit pattern that substantially prevents unraveling and preserves the stability of the mesh or scaffold device, especially when the mesh or scaffold device is cut. An example scaffold device employs a knitted mesh including at least two yarns laid in a knit direction and engaging each other to define a plurality of nodes.

A method of using a biocompatible surgical knitted, silk scaffold device in a breast augmentation or in s breast reconstruction cosmetic or surgical procedure such as single-stage or two-stage breast reconstruction. In an aspect of the invention, the silk scaffold employs a knit pattern that substantially prevents unraveling and preserves the stability of the mesh or scaffold device, especially when the mesh or scaffold device is cut. An example scaffold device employs a knitted mesh including at least two yarns laid in a knit direction and engaging each other to define a plurality of nodes. The at least two yarns include a first yarn and a second yarn extending between and forming loops about two nodes. The second yarn has a higher tension at the two nodes than the first yarn. The second yarn substantially prevents the first yarn from moving at the two nodes and substantially prevents the knitted mesh from unraveling at the nodes.

A method of using a biocompatible surgical knitted, silk scaffold device in a breast augmentation or in a breast reconstruction cosmetic or surgical procedure such as single-stage or two-stage breast reconstruction. In an aspect of the invention, the silk scaffold employs a knit pattern that substantially prevents unraveling and preserves the stability of the mesh or scaffold device, especially when the mesh or scaffold device is cut. An example scaffold device employs a knitted mesh including at least two yarns laid in a knit direction and engaging each other to define a plurality of nodes. The at least two yarns include a first yarn and a second yarn extending between and forming loops about two nodes. The second yarn has a higher tension at the two nodes than the first yarn. The second yarn substantially prevents the first yarn from moving at the two nodes and substantially prevents the knitted mesh from unraveling at the nodes.

A method for producing a virtual forecasted model of a breast augmentation subject, comprising, receiving a preoperative subject's scanned image, wherein the scanned image comprises a three dimensional image, converting the scanned image from a scanned image format to a VRML image format, importing the converted VRML image into a VRML image editor, receiving, from a breast implant database, at least one modeled virtual breast implant, wherein the received virtual breast implant is selected based on a desired actual breast implant that is to be implanted in the preoperative subject, and embedding the received virtual breast implant in the preoperative subject's converted VRML image.

A method is disclosed for preparing a soft tissue site, and augmenting the soft tissue site, such as the breast(s) of a subject through use of devices that exert a distractive force on the breast(s) and grafting of autologous fat tissue such as domes with sealing rims for surrounding each of the breasts and a regulated pump. The method for preparing the soft tissue site, and enhancing fat graft results, entails application of the distracting force to the targeted soft tissue site for several weeks prior to the graft procedure. A related aspect of the invention includes following the preparation steps by transfer of fat from other areas of the subject to the subject's breast(s), and then reapplication of the distractive force to the breast(s) that received the autologous fat graft. Alternatively, fat from genetically related sources may be used, and the fat may be further processed prior to injection. Substantial breast augmentation, high rates of graft survival and negligible graft necrosis (data demonstrating 80% survival and only 20% necrosis is presented) or calcification result from the practice of these methods.

A breast-supportive and breast-positioning brassiere designed to be used postoperatively by patients including obese patients and fuller-sized women who have undergone cardiothoracic surgery that requires a mid-sternal incision (sternotomy). The brassiere is also for other interventions in the thoracic region, when a comfortable and efficient individual positioning and support of the breast(s) would be desirable; an example being to prevent symmastia after breast augmentation surgery. The brassiere prevents gravitation of the breast tissue to the lateral sides, keeps the breast tissue away from the mid center, and supports the weight of the breasts. The brassiere is designed to promote less pain, less wound complications, esthetically improved wound healing, less heat generation, improved wound inspection and access for wound care, while maintaining support and dignity.

A one-step real-time system for treating, reconstructing or augmenting a breast tissue defect in a patient comprising means for extracting adipose tissue, isolate adipocytes, process and re-inject stem and regenerative cells to the breast of the patient.

An augmented reality imaging system for cosmetic surgical procedures. In a breast augmentation procedure, a virtual breast image is generated and overlaid on a target marker covering a patient's real breasts such that the patient can see her real body with virtual breasts at the location of her real breasts. The patient views this augmented reality image on a mobile device such as a tablet computer. By use of low polygon graphics and a set of artistic sliders on the mobile device, a surgeon can manipulate and deform the virtual breasts in real time to produce lifelike outcomes of various surgical options.

A method and instruments for performing breast augmentation mammaplasty in a patient are provided. The method includes making an incision to gain access to an area underneath the breast of the patient, and providing a retractor including a shaft and a tubular member connected to the shaft. The tubular member includes a hollow endoscope guide portion and a generally flattened blade portion, where the endoscope guide portion transitions into the blade portion such that an end of the blade extends beyond an end of the endoscope guide. The method further includes inserting the retractor at least partially through the incision to aid in placing a breast implant within the patient.

A method and apparatus for the preoperative estimation of breast implant volume, In which a volume of air, water, or other substance is used to inflate one or more bladders located within the cups of the brassiere-like garment. The apparatus is operated by pumping an amount of air from the outside atmosphere, or water or another substance from a reservoir or external water supply, into the bladders, according to the patient's preference as to the size of breasts she desires. A gauge is used to measure the capacity of each bladder when inflated to its desired size. The volume of each bladder as measured by the gauge can then be used to determine the size of breast implant to be used during breast augmentation surgery.

Breast fixation devices for use in breast reconstruction and breast augmentation limit the rotation or movement of breast implants after implantation that results in an unnatural appearance of the breast. The breast fixation devices can include a thin-walled enclosure in the shape of a pouch. A breast implant is secured inside the pouch to limit movement by applying compression to the breast implants, or using a mating or interlocking mechanism between the pouch and breast implant. The pouches containing the breast implants are implanted in the breast. Tissue in-growth into the pouch limits movement of the pouch-breast implant assembly and thereby limits rotation, migration, and displacement of the breast implant. The pouches preferably comprise poly-4-hydroxybutyrate or copolymer thereof.

A breast implant device product that mimic the natural pectoral fat pad of the breast and is characterized by an incomplete pyramid with isosceles triangular base and wedge-shaped edges and sloping faces that meet at acute angles with variable degree located medially, laterally and on the top and a footprint characterized by a semicircular lower portion and an oval paraboloid upper portion and a center of gravity located closer to the base than to the profile, the said footprint is advantageously converging and moving towards the underlying surface as the chest wall with a method of manufacturing and a method of use of the said implant including a breast pyramid sizing system.

A functional garment comprises a first breast cup and a first cross strap, two opposite ends of which are attached to the inner and outer edges of the first breast cup, respectively. The functional garment can be used to simultaneously provide both orthopedic and breast augmentation benefits. A plurality of countervailing forces simultaneously provide force on the shoulders, to bring them back and / or the shoulder blades closer together, and the breasts, to bring them closer together and / or lift them.

A method and instruments for performing breast augmentation mammaplasty in a patient are provided. The method includes making an incision to gain access to an area underneath the breast of the patient, and providing a retractor including a shaft and a tubular member connected to the shaft. The tubular member includes a hollow endoscope guide portion and a generally flattened blade portion, where the endoscope guide portion transitions into the blade portion such that an end of the blade extends beyond an end of the endoscope guide. The method further includes inserting the retractor at least partially through the incision to aid in placing a breast implant within the patient.

The invention discloses a complex for increasing breast volume and a preparation method of the complex. The complex is prepared from the following components in percentage by weight: 0.045 to 0.055 percent of acetyl hexapeptide-18, 0.5 to 1 percent of kudzuvine root extract, 0.2 to 0.4 percent of sodium hyaluronate, 4 to 6 percent of glycerol, 0.3 to 0.5 percent of butanediol, 0.3 to 0.5 percent of 1,2-hexanediol, and the balance of purified water. The complex prepared by the invention can be prepared into beauty products such as breast augmentation cream and breast augmentation essence, has efficacy of promoting increase of the breast volume, and enables breast to be plumper.