In a method of making a breast prosthesis for use by a wearer having a body temperature, a plurality of dissolvable beads is placed into an open back of a breast-shaped mold. The open back of the mold is sealed. A suspension of an uncured silicone rubber liquid and a plurality of phase change material pellets is injected into the mold around the beads. The uncured silicone rubber is allowed to cure, thereby forming a breast shape. The phase change material has a latent heat of fusion at a melting point so as to remove heat from the wearer when the body temperature is at least at the melting point. The breast shape is removed from the mold and the dissolvable beads are dissolved from the breast shape.

Embodiments of brassieres with prosthesis for mastectomy patients are described herein. Other embodiments may be described and claimed.

Embodiments of brassieres with prosthesis for mastectomy patients are described herein. Other embodiments may be described and claimed.

A passive stent for retaining an organ in an expanded state configured to adhere and substantially conform to an external surface of the organ may include an inner layer, an outer layer, and a middle layer that is enclosed by the inner layer and the outer layer, comprising a plurality of components configured to interlock and maintain the organ in an expanded state upon application of a vacuum. A method for retaining an organ in an expanded state may include applying at least one force to the organ to place the organ in the expanded state; applying a passive stent to an external surface of the organ; and applying a vacuum to the passive stent sufficient to cause a plurality of components of at least one layer of the passive stent to interlock, where the at least one layer is configured to maintain the organ in the expanded state after interlocking.

Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and/or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the in-growth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy/breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast.

Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and/or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the in-growth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy/breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast.

The present disclosure relates generally to devices and methods to relieve tension or stress on tissue and, in particular, tissue that includes a surgical incision site. A shape-setting material is used to conform the device to the tissue without the need for continuous application of negative pressure. The device can support and improve the health of breast tissue after breast augmentation or reconstruction post-mastectomy.

A garment having integrated prosthetic breasts is disclosed. The garment includes an inner front layer, a middle component which includes at least one, and ideally two prosthetic breast members. The prosthetics are lightweight so that no elastic across the torso is needed. An outer front layer covers the middle component. The middle component is formed of a mesh layer which is sewn to the inner front layer only at the neckline and arms, and has an open bottom edge. The prosthetic breast members are attached to the mesh layer and provide shaping for mastectomy patients or other individuals having a need or desire for natural looking shaping.

A garment having integrated prosthetic breasts is disclosed. The garment includes an inner front layer, a middle component which includes at least one, and ideally two prosthetic breast members. The prosthetics are lightweight so that no elastic across the torso is needed. An outer front layer covers the middle component. The middle component is formed of a mesh layer which is sewn to the inner front layer only at the neckline and arms, and has an open bottom edge. The prosthetic breast members are attached to the mesh layer and provide shaping for mastectomy patients or other individuals having a need or desire for natural looking shaping.

A breast prosthesis device and method for making same are disclosed. The prosthesis has an inner wall mesh having a first density. The inner wall mesh is configured to align with a chest wall of the user. The prosthesis has an outer wall mesh having a second density. The outer wall mesh configured to have an ideal shape for the user. The prosthesis may also have a band with a density greater or equal to the inner and outer wall meshes. The prosthesis has a central portion disposed in between the inner and outer wall meshes. The prosthesis can be generated using 3D scans of the user manipulated such that the resulting structure mimics human tissue.