The present invention relates to a delivery system for surgically implanting an implant prosthesis, particularly to a sterile implant delivery system.
Various devices are known for delivery of an implant into a surgical pocket, including implantation of a flexible implant prosthesis, including, for example, a breast implant, a calf implant, a pectoral implant, a buttocks implant, a chin implant, a tissue expander, or other known flexible implant prosthetic devices. These devices are delivered separately and are assembled at the time of use in an operating theater. In general, the surgical theater is normally as sterile as possible, but it is nevertheless not unusual for sterility to be compromised during a surgical procedure involving many surgical personnel. Despite that many steps may have been taken to avoid loss of sterility and to provide antibiotics and other medicines to mitigate any such loss of sterility, problems resulting from non-sterile conditions continue in the surgical arts, particularly where long-term prosthetic devices are to be implanted.
The present invention addresses the problems of lack or loss of sterility of implanted flexible prosthetic devices, and provides for a significantly improved sterility of such flexible prosthetic devices.
Accordingly, in one embodiment, there is provided a delivery system for inserting an implant into a surgical pocket, including a flexible sleeve having a first end and a second end and being sealed around its entire outer periphery forming an interior space, wherein the flexible sleeve is tapered toward at least one of the first end and the second end; and an implant contained and sealed within the interior space; in which the interior space and the implant contained and sealed therein are in a sterile condition. In one embodiment, the implant contained and sealed within the flexible sleeve is provided from the manufacturer in a sterile condition, both externally and, particularly, internally, so that when it is opened for use, the entire contents of the device, including the implant, are sterile and can remain so throughout the surgical procedure. By providing the system in a sterile condition, the likelihood of contamination during the surgical implantation procedure is significantly reduced.
The present invention may be useful with a variety of types of surgically implanted devices. The annexed drawings are intended to provide a nonlimiting depiction of examples of an apparatus and to demonstrate the disclosed process, for the purpose of providing a better understanding of the invention, and are not intended to be limiting in any way. In the annexed drawings, like parts and features may have like or corresponding reference numerals. It should be appreciated that for simplicity and clarity of illustration, elements shown in the Figures have not necessarily been drawn to scale. For example, the dimensions of some of the elements may be exaggerated relative to each other for clarity.
The foregoing Figures are provided as non-limiting examples of embodiments of the present invention, and are intended to facilitate understanding of the present invention.
Surgical implants, and particularly breast implants, have been in use for over 40 years, and the implants and devices and methods for surgically inserting such implants have gradually evolved. However, some issues, as particularly relevant here, relating to possible contamination and the needed sterility of the implants, have remained. Recently, there has been a preference for minimal handling of implants during implantation, which is sometimes referred to as a “touchless technique”. The present invention includes the ability to provide for producing and shipping the implant packaged in a plastic bag or flexible sleeve that is suitable for use as a funnel for inserting the implant into a surgical pocket. In one embodiment, the flexible sleeve is manufactured with an implant-compatible lubricant within the bag. Thus, the implant is provided from the manufacturer already in a sealed bag forming a flexible sleeve with both the implant and at least the interior of the bag or flexible sleeve in a sterile condition. Of course, the entirety of the delivery system should be maintained in a sterile condition, both externally and internally. To facilitate this sterility, the delivery system is provided by the manufacturer in a suitably configured packaging designed to maintain the delivery system in a sterile condition. For example, implants may be placed in double packaging that ensures a dual microbiological barrier, to maintain sterility until implantation. The double packaging is delivered to the end user in a cardboard box that provides additional protection to provide the delivery system in the best possible condition.
In various embodiments, the flexible sleeve is shaped like a hexagon, a diamond, a cone, or a trapezoid shape, preferably in an elongated form. Other shapes may also be used, but it is considered that the hexagonal, diamond, trapezoidal or conical shapes, particularly any of these in an elongated form, are the most likely to be preferable. The shape should include at least one sufficiently tapered end to provide for cutting to form an opening of a suitable size for use as an outlet of the flexible sleeve, to create a funnel, for delivering the implant into a surgically formed pocket through the smallest possible incision. These features are described in more detail in the following description of various example embodiments of the invention.
In one embodiment, the flexible sleeve includes a valve or access port at one end of the bag, for example, on one side or end. The access port allows the surgeon or assistant to instill one or more of an antibiotic solution, an antibacterial, an antimicrobial, a lubricant, a gas, water, and/or a saline or other solution of the surgeon's choice into the bag. The valve or access port can be a needleless valve, or it can be a self-sealing seal suitable for penetration by a needle.
In one embodiment, on one or more corner or end of the bag are formed markings which show locations suitable for cutting to form an opening to modify the bag into a flexible sleeve that allows the implant to be squeezed out of the bag. In a process of implanting the device, the surgeon or assistant will cut the corner of the bag at the appropriate mark to allow the implant to be squeezed out of the bag without damaging the implant, place the opening of the bag into an incision forming a surgical pocket and then squeeze the flexible sleeve to thereby push the implant out of the flexible sleeve and into the surgical pocket. The flexible sleeve formed by cutting a corner or end off the sealed flexible sleeve will then be similar to the funnels and assist sleeves available in the prior art. Once the implant is in place in the surgical pocket, the bag is removed.
Thus, in one embodiment, the surgeon or assistant never directly touches the implant and the implant will never have touched the skin of the patient or any portion of the operating theater. The surgeon will of course need to use the usual care if the implant required adjustment within the surgical pocket so as not to contaminate the implant with skin or other flora that may be present.
Additional details relating to various embodiments of the present invention are set forth in the following detailed description.
In one embodiment, the delivery system for inserting an implant into a surgical pocket includes:
a flexible sleeve having a first end and a second end and being sealed around its entire outer periphery forming an interior space, wherein the flexible sleeve is tapered toward at least one of the first end and the second end; and
an implant contained and sealed within the interior space;
wherein the interior space and the implant contained and sealed therein are in a sterile condition. Of course, the outer surfaces of the delivery system should also be sterile, and the delivery system will normally be provided packaged within a sterile container, bag, envelope or other suitable packaging.
Referring now to
The flexible sleeve 102 shown in
As schematically depicted in
As shown in
In the embodiment of
It is noted that the embodiment depicted in
Referring now to
The flexible sleeve 202 shown in
As shown in
In the embodiment of
It is noted that the embodiment depicted in
In one embodiment, the flexible sleeve 102, 202 is formed of a material which is sufficiently flexible, but which is also sufficiently strong to withstand the pressures applied during use, and which also enables portions of the flexible sleeve 102, 202 to be flattened as much as possible, considering that the implant 104 is contained and sealed within the flexible sleeve 102, 202 during shipping and storage prior to use.
Referring now to
In accordance with various embodiments of the present invention, the flexible sleeve 102, 202 is made of a flexible material. In one embodiment of the invention, the flexible sleeve 102, 202 can be provided by a non-woven fabric material such as a plastic-containing a non-woven fabric which is pliable yet resistant to stretching. It is also envisioned that use of a transparent plastic or other suitable polymer material which has sufficient properties including flexibility and non-elasticity may be used. It is considered that there are advantages to using a transparent or semi-transparent material to assist the surgeon in proper orientation of the implant 104 within the interior of the flexible sleeve 102, 202. Suitable transparent materials may include Mylar® brand of plastics, plastics made from Tygon® brand of plastics, vinyls, polyvinyl chloride, and other similar materials.
In one embodiment, suitable materials which are both flexible and transparent include compositions of ethylene and alpha-olefin copolymers such as the compositions used in IV saline bags. Suitable multilayer films and sealed structures are taught in U.S. Pat. Nos. 6,743,523 and 7,267,885 both of which are incorporated herein by reference for their teachings relating to suitable films for IV bags, which may also be useful with the present invention, and which may be consulted for additional details. As disclosed therein, suitable films heat sealed around their entire periphery to form suitable containers, are transparent with minimal hazing, and can be sterilized using gas sterilization or heat with intact seals and remain sufficiently flexible and pliable for the necessary manipulation described herein.
As noted, in accordance with embodiments of the present invention, the delivery systems 100, 200 can be provided in a sterile condition, with the implant 104 already inside the flexible sleeve 102. Accordingly, the material from which the flexible sleeve is made should be capable of withstanding at least one of several conventional sterilization techniques such as a steam autoclave, chemical gas sterilization, or irradiation.
In one embodiment, the interior surface of the flexible sleeve 102, 202 is provided with a low coefficient of friction to facilitate passage of the implant 104 through the flexible sleeve 102, 202 at the time the implant is to be transferred into the patient's surgical cavity.
In one embodiment, a surgically appropriate lubricant can be either included within the flexible sleeve 102, 202 at the time of manufacture, or can be injected into the interior of the flexible sleeve 102, 202 just before or during the surgical procedure in which the implant 104 will be squeezed out of the flexible sleeve for placement into the surgical pocket. The lubricant will facilitate passage of the implant 104 through the interior of the flexible sleeve. Such lubricants, if placed into the flexible sleeve during manufacture, should be sufficiently stable or inert to the sterilization conditions applied to the flexible sleeve 102, 202 and the implant 104 as part of the manufacture process. It is noted that other materials that may be present or injected into the flexible sleeve can act as a lubricant, and thus it may not be necessary to add a separate lubricant.
Since the size of the implant 104 may vary in a range from about 100 cc to about 800 cc, or larger for other types of implants, the plurality of lines 110 can be used to estimate an appropriate location that the flexible sleeve 102, 202 is to be cut to form an opening to accommodate and allow passage of various size implants 104. It is noted that the indicia 110 are schematically depicted in
In one embodiment, the flexible sleeve 102, 104 is provided with an inner liner (not shown) which may be present within the interior of the flexible sleeve 102, 202. Such a liner may be integral with the interior surface of the flexible sleeve 102,202 or may be a separate layer of material inserted within the interior of the sleeve 102, 202 at the time of manufacture.
As described above, in various embodiments, the flexible sleeve 102, 202 further includes a valve configured for insertion of a fluid into the flexible sleeve.
As described above, in one embodiment the flexible sleeve 102, 202 includes one or more indicia formed across the first end, the second end or both the first end and the second end, the indicia configured to indicate sites at which the flexible sleeve is to be cut to form an opening from which the implant is squeezed out of the flexible sleeve into a surgical pocket during a surgical procedure. In various embodiments, locations of the indicia correlate to size of the implant.
As described above, in various embodiments, the flexible sleeve 102, 202 is transparent or semi-transparent.
As described above, in various embodiments, the delivery system 100, 200 and its contents are sterilized during manufacture.
In various embodiments, the implant is a breast implant. In one embodiment, the breast implant is a prefilled silicone breast implant. In another embodiment, the breast implant is a saline breast implant in a flattened condition and configured to be filled with saline. Such breast implants are known in the art, and are not further described herein for that reason and for brevity.
As described above, in some embodiments, the flexible sleeve further includes in its interior with the implant one or more of an antibiotic solution, an antibacterial, a lubricant, a gas, water, and/or a saline or other solution.
As will be recognized, various embodiments of the present invention are applicable to silicone breast implants. When embodiments of the present invention are used for tissue expanders or saline implants, the expander or implant will need to have an appropriate fill tube attached to the expander or implant itself prior to that implant being sealed and sterilized at the manufacturing plant. As will be recognized by the skilled person, squeezing a deflated saline implant or expander out of the bag might be more difficult and post placement adjustment of the implant or expander in the pocket might be required. Alternatively, the implant or tissue expander could be partially filled either at the time of manufacture or at the time of use. Even with this additional step at the time of surgery, embodiments of the delivery system of the present invention will still reduce or eliminate exposure of the implant or expander during handling and will reduce exposure to the operating room environment as compared to current devices and procedures.
In one embodiment, the present invention further provides a method of making a delivery system for inserting an implant into a surgical pocket, including the steps of providing an implant; providing a flexible sleeve having a first end and a second end and an outer peripheral edge, wherein the flexible sleeve is tapered toward at least one of the first end and the second end, and at least a portion of the flexible sleeve is unsealed; inserting an implant into the flexible sleeve, sealing the outer peripheral edge completely around the flexible sleeve; and sterilizing the delivery system after the inserting and the sealing. Suitable materials and methods for making and sealing multilayer films suitable for use as the flexible sleeve are taught in U.S. Pat. Nos. 6,743,523 and 7,267,885, which may also be useful with the present invention, and which may be consulted for additional details on the methods.
In one embodiment, the present invention further provides a method of inserting an implant into a surgical pocket in a patient, including the steps of providing a delivery system, the delivery system including a flexible sleeve containing an implant and having a first end and a second end, the flexible sleeve being sealed around its entire outer periphery, wherein the flexible sleeve is tapered toward at least one of the first end and the second end, and wherein the flexible sleeve is in a sterile condition at least in its interior; during a surgical procedure, cutting the flexible sleeve across at least one of the first end and the second end to form at least one opening; applying manual pressure to squeeze the implant out through one of the at least one opening and into the surgical pocket. In one embodiment, the method of inserting an implant further includes inserting one or more of an antibiotic solution, an antibacterial, a lubricant, a gas, water, or a saline or other solution into the flexible sleeve prior to the applying manual pressure step. In one embodiment, the method of inserting an implant further includes activating a lubricant that is already present in the flexible sleeve together with the implant.
The following numbered clauses provide further support for the presently disclosed and claimed invention.
Clause 1. A delivery system for inserting an implant into a surgical pocket, comprising:
a flexible sleeve having a first end and a second end and being sealed around its entire outer periphery forming an interior space, wherein the flexible sleeve is tapered toward at least one of the first end and the second end; and
an implant contained and sealed within the interior space;
wherein the interior space and the implant contained and sealed therein are in a sterile condition.
Clause 2. The delivery system of clause 1, further comprising a valve configured for insertion of a fluid into the flexible sleeve.
Clause 3. The delivery system of either of clause 1 or 2, wherein the flexible sleeve includes one or more indicia formed across the first end, the second end or both the first end and the second end, the indicia configured to indicate sites at which the flexible sleeve is to be cut to form an opening from which the implant is squeezed out of the flexible sleeve into a surgical pocket during a surgical procedure.
Clause 4. The delivery system of clause 3, wherein locations of the indicia correlate to size of the implant.
Clause 5. The delivery system of any one of clauses 1-4, wherein the flexible sleeve is transparent or semi-transparent.
Clause 6. The delivery system of any one of clauses 1-5, wherein the delivery system and its contents have been sterilized during manufacture.
Clause 7. The delivery system of any one of clauses 1-6, wherein the implant is a breast implant.
Clause 8. The delivery system of clause 7 wherein the breast implant is a prefilled silicone breast implant.
Clause 9. The delivery system of clause 7 wherein the breast implant is a saline breast implant in a flattened condition and configured to be filled with saline.
Clause 10. The delivery system of any one of clauses 1-9, wherein the flexible sleeve further comprises in its interior with the implant one or more of a lubricant, an antibiotic, an anti-bacterial composition, a gas, and water.
Clause 11. A method of making a delivery system for inserting an implant into a surgical pocket, comprising:
providing an implant;
providing a flexible sleeve having a first end and a second end and an outer peripheral edge, wherein the flexible sleeve is tapered toward at least one of the first end and the second end, and at least a portion of the flexible sleeve is unsealed;
inserting an implant into the flexible sleeve,
sealing the outer peripheral edge completely around the flexible sleeve; and
sterilizing the delivery system after the inserting and the sealing.
Clause 12. A method of inserting an implant into a surgical pocket in a patient, comprising
providing a delivery system, the delivery system comprising:
a flexible sleeve containing an implant and having a first end and a second end, the flexible sleeve being sealed around its entire outer periphery, wherein the flexible sleeve is tapered toward at least one of the first end and the second end, and wherein the flexible sleeve is in a sterile condition at least in its interior;
during a surgical procedure, cutting the flexible sleeve across at least one of the first end and the second end to form at least one opening;
applying manual pressure to squeeze the implant out through one of the at least one opening and into the surgical pocket.
It should be appreciated that the process steps and structures described below do not form a complete process flow for manufacturing items such as the flexible sleeves and delivery systems described herein. The present invention can be practiced in conjunction with fabrication techniques currently used in the art, and only so much of the commonly practiced process steps are included as are necessary for an understanding of the present invention.
While the principles of the invention have been explained in relation to certain particular embodiments, and are provided for purposes of illustration, it is to be understood that various modifications thereof will become apparent to those skilled in the art upon reading the specification. Therefore, it is to be understood that the invention disclosed herein is intended to cover such modifications as fall within the scope of the appended claims. The scope of the invention is limited only by the scope of the appended claims.
The present application is related to and claims benefit under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 62/414,064, filed 28 Oct. 2016, the entirety of which is incorporated herein by reference.
Number | Date | Country | |
---|---|---|---|
62414064 | Oct 2016 | US |