The present invention relates to a medical support device for supporting a breast implant or breast tissue, and relates in particular to a medical support device, which comprises a pre-shaped, three-dimensional, generally hemispherical, synthetic and preferably resorbable mesh structure having a number of portions with individual and specific mechanical characteristics.
A medical breast reconstruction is a procedure that typically involves the use of prosthetic breast implants, e.g. silicone or saline implants, which are placed either below or above the breast muscle, to recreate a female breast. In other, also common techniques, the patient's own body tissue can be used to reconstruct a breast. Within the art of reconstructive and cosmetic breast surgery it is further common to at least partly place the artificial implant or the patient's body tissue in a support device.
Examples of such support devices are disclosed in U.S. Patent Publication No. 2013/0253645 A1 to Kerr et al. In this publication, a three-dimensional medical support device is disclosed, which preferably is knitted from polymeric yarns, threads, filaments or monofilaments and which, at a given location in the device, can have an elongation of 0-30% along a horizontal axis and an elongation of 0-10% along a vertical axis, which is said to give a vertical support against gravity and the force of landing during walking and running and also to give a horizontal support which makes the implant more comfortable and allows a reconstructed breast to appear and feel more natural.
As recognized in the prior art, support, comfort as well as appearance and feeling of a supported, reconstructed breast are important features of a medical support device for supporting a breast implant or breast tissue; and although efforts have been made to provide a support device with corresponding characteristics, there is still a need for an improved support device, which provides better support for an artificial breast implant or bodily tissue and which also stimulates integration with the existing tissue at the implant site.
A medical support device according to the present invention is intended to support and optionally also lift natural tissue or artificial material used to reconstruct a female breast structure. In one embodiment, a support device comprises a generally hemispherical, cone- or cup-shaped three-dimensional structure comprising a mesh structure, which can be made from non-biodegradable or preferably biodegradable polymeric material. In another embodiment, a support device comprises approximately one half of a generally hemispherical, cone- or cup-shaped three-dimensional structure comprising a mesh structure, which can be made from non-biodegradable or preferably biodegradable polymeric material. According to the invention, the hemispherical or semi-hemispherical three-dimensional structure is further divided into two, three or more portions with different mechanical properties. Typically, a lower portion (as seen in implanted state) of a three-dimensional mesh structure can be rather inelastic, i.e. having a high modulus of elasticity, and have high strength to provide a lot of support for the implanted breast material, while an upper portion (as seen in implanted state) of a three-dimensional mesh structure can be more elastic, i.e. have a low modulus of elasticity, and have less strength to provide more comfort for the person having a reconstructed breast.
a shows a front view and
a shows a front view and
a shows a front view and
The present invention relates to a medical support device for supporting a (typically female) breast after a medical breast reconstruction surgery. A breast reconstruction surgery generally involves the re-creation of a breast either by using the patient's own tissue and/or using an artificial medical implant made from, e.g., silicone or saline.
For this purpose, the implanted material can be held in place with a three-dimensional, generally hemispherical, cup-shaped or cone-shaped support device, which can be made from degradable or non-degradable mesh material. For some medical cases, approximately one half of a generally hemispherical, cup-shaped or cone-shaped support device can be sufficient to provide the desired support for the implanted reconstruction material; and also other sizes and shapes of a three-dimensional mesh structure suitable for supporting a reconstructed breast are within the scope of the present invention.
Support devices of this kind are known in the art; and are, for example, disclosed in the above-referenced patent document. However, the inventor of the present invention has realized that the mechanical requirements regarding, e.g., strength, elasticity and stability, are not uniformly distributed over the surface of a three-dimensional, generally hemispherical support device used for supporting a reconstructed breast. Instead, typically more support is required at a lower part of the support device, whereas an upper part of the support device should be more mechanically compliant to provide the patient with as much comfort as possible and also to give the reconstructed breast a natural appearance. It can be noted that strictly speaking, terms herein like “lower” or “bottom” and “upper” or “top” refer to a medical support device in its implanted state, but the meaning should nevertheless be obvious for the person skilled in the art.
A first example of a medical support device according to the present invention is schematically depicted in
As has been indicated above, the most basic mechanical requirements on the lower portion 11 are to support and hold an implant or implanted tissue in place, which otherwise has a tendency to become dislocated, i.e. typically move downwards due to gravitation. Therefore the lower portion 11 is characterized by having a high modulus of elasticity (being rather inelastic) and/or having a high degree of stiffness, strength and/or stability. For the upper portion 13 the situation is different, since the mechanical requirements regarding elasticity, strength and stability are lower. The upper portion 13 of the mesh structure 10 should instead be comfortable for the person having a reconstructed breast and should also provide the breast with a natural and appealing overall appearance. Hence, the upper portion 13 is characterized by having a comparatively low modulus of elasticity (being rather elastic) and being compliant and/or having a low degree of stiffness, strength and/or stability. The mechanical requirements for the intermediate portion 12 are somewhere in between the mechanical requirements for the lower portion 11 and the upper portion 13; and the intermediate portion 12 is consequently characterized by having moderately high modulus of elasticity and having a moderate compliance and/or having a moderately high degree of stiffness, strength and/or stability. In this embodiment, there are three portions 11, 12 and 13 indicated in
A second embodiment of a medical support device according to the present invention is disclosed in
A somewhat different division into portions with different mechanical characteristics is disclosed in a third embodiment of a medical support device according to the present invention. This embodiment is presented in
Different techniques can be utilized to produce a medical support device according to the present invention. For example, in knitting or weaving techniques, knitting or weaving patterns can be changed from one portion to another, e.g. by varying pore sizes or number of fibers per surface area or include more fibers with higher modulus of elasticity It is also possible to sew or otherwise join together different mesh portions having different mechanical properties, or even for some portions arrange two or more layers of mesh on top of each other. To create the three-dimensional shape, i.e. to produce the hemispherical cup-shape, meshes are commonly heat treated. This process, which in the art also is referred to as annealing, means that mesh material is exposed to heat, typically by placing the mesh material in a mould which is heated to a specific temperature. With suitable choice of material, e.g. polymeric material, the mesh material and thereby the medical support device will adopt the shape of the mould. To produce portions with different mechanical characteristics, certain areas of the mesh material can be exposed to more heat, i.e. higher temperature or longer dwell time in the mould. For example, with reference back to the third embodiment described in conjunction with
The bands or stripes 83 are used for fastening of the support device to soft tissue at the implant site. Sutures, e.g. degradable sutures, can be used to attach the bands or stripes 83 to the soft tissue. Once fastened, the support device can act to lift the tissue which it supports. The support device is further provided with a set of strings 84, which are used to adjust the shape and size of the support device, to match the size of the patient's natural breast size, or according to the patient's desire.
For the device illustrated in
As indicated above, one mechanical property that can characterize a mesh structure according to the invention is extension. Extension is preferably measured using the
ASTMD D3787-1 guideline for ball burst strength, with some preset parameters, such as a preload of 0.1 N and a test speed of 75 mm/min. As a non-limiting example, the extension (travel distance of the ball) measured at a load of 50 N can for a bottom or lower portion, which is characterized by having a high modulus of elasticity, a high degree of stiffness, strength and/or stability, be in the interval of 2 mm to 10 mm, while an upper or top portion, which is characterized by having a comparatively low modulus of elasticity and being mechanically compliant and/or having a low degree of stiffness, strength and/or stability, be in the interval of 5 mm to 15 mm. Intermediate portions of a mesh structure can have values between these two intervals.
Although the present invention has been described with reference to specific embodiments, also shown in the appended drawings, it will be apparent to those skilled in the art that many variations and modifications can be done within the scope of the invention as described in the specification and defined with reference to the claims below.
This application claims priority from U.S. Provisional Patent Application No. 61/966,998, filed on Mar. 7, 2014, the entire contents of which are incorporated herein by reference.
Number | Date | Country | |
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61966998 | Mar 2014 | US |