Abstract
A surgical implant, which in use, provides a barrier between layers of tissue such that tissue on one side of the implant does not adhere to tissue on the other side, the implant being made of suitably anatomically shaped surgically acceptable sheet material.
Claims
1. A surgical implant consisting of a biologically inert material; wherein said implant is elastic, wherein said implant has a thickness of less than 0.5 mm, wherein said implant is a pre-shaped three dimensional concave structure so as to conform to a temporo-parietal lobe or a frontal lobe of a cranium without kinks or overlap such that, in use, the pre-shaped three dimensional concave structure of said implant assists the implant to remain in place in a cranial defect; wherein the biologically inert material is one of a medical grade flexible silicone film or a medical grade flexible PTFE film; wherein, in use, the implant provides a barrier between layers of tissue that contact respective sides of the implant such that tissue on one side of the implant does not adhere to tissue on an opposite side of the implant, and wherein, in use, the implant flexes to accommodate a swelling brain.
2. The implant of claim 1, wherein the biologically inert material is a single layer of medical grade flexible PTFE film.
3. The implant of claim 1, wherein the biologically inert material is a single layer of medical grade flexible silicone film.
4. The implant of claim 1, wherein the implant is reinforced in peripheral areas for suture retention or the implant contains fixation sites that allow sutures screws or rivets to be used to secure the implant to surrounding hard or soft tissues.
5. The implant of claim 1, wherein the implant further includes enclosed channels accessible via apertures or probes to deliver therapeutic substances to the brain and associated tissues.
6. The implant of claim 1, wherein the implant further includes a network of channels that allow closed circulation of fluid to and from an external device incorporating a positive or negative pressure pump.
7. The implant of claim 1, wherein the implant comprises a network of channels to and from an incorporated port or reservoir.
8. A surgical method including the steps of: (a) providing an implant according to claim 1; and (b) fitting the implant to the tempero-parietal or frontal lobe of a skull.
Description
BRIEF DESCRIPTION OF THE FIGURES
(1) FIG. 1 is a representation of implants suitable for procedures on the temporo-parietal lobe of a human cranium.
(2) FIG. 2 is a representation of an implant suitable for procedures on the frontal lobe of a human cranium.
(3) FIG. 3 is a representation of an implant according to an embodiment of the present disclosure.
(4) FIG. 4 is a representation of an implant including reinforcement in peripheral areas and/or fixation sites.
(5) FIG. 5 is a representation of an implant incorporating pharmaceutical compositions.
(6) FIG. 6 is a representation of an implant including a monitoring probe.
(7) FIG. 7 is a representation of an implant incorporating slow release biodegradable substances.
(8) FIG. 8 is a representation of an implant including an enclosed channel accessible via apertures or probes.
(9) FIG. 9 is a representation of an implant including a network of channels allowing closed circulation of fluid.
(10) FIG. 10 is a representation of an implant including a semi-permeable membrane.
(11) FIG. 11 is a representation of an implant including a network of channels to and from an incorporated port or reservoir.
DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENT OF THE INVENTION
(12) The invention will now be described with reference to the following non limiting illustration.
(13) FIGS. 1 and 2 show implants 1, 2 suitable for temporo-parietal and frontal lobe use on a skull, respectively. The surgeon uses standard surgical techniques to fit the implant however it should be noted that compared to using a flat sheet the pre-shaped and pre-contoured implant of the present invention is simpler to fit, saves operating theatre time and minimizes discomfort as a flat sheet may buckle or overlap. Further, the curved nature of the implant of the present invention means that it is more likely to remain in place in the defect. A flat sheet may buckle or overlap and cause discomfort and make a second procedure necessary. As can been seen from the photographic depiction of the example implants of FIGS. 1 and 2, the example implants are three dimensional concave structures configured to conform to a temporo-parietal lobe and a frontal lobe of a cranium, respectively, without kinks or overlap. As can be seen from the photographic depiction of the example implants of FIGS. 1 and 2, the example implants are three dimensional concave structures configured to conform to a temporo-parietal lobe and a frontal lobe of a cranium, respectively, without kinks or overlap.
(14) FIG. 3 shows an implant 3 consistent with disclosed embodiments.
(15) FIG. 4 shows an embodiment of implant 3 that includes a plurality of areas 4. Areas 4 may be reinforcement areas and/or fixation sites.
(16) FIG. 5 shows that implant 3 may incorporate one or more pharmaceutical compositions 5, such as antibiotics and anti inflammatory compounds. Such agents may be introduced via material porosity or via the incorporation of a second material with such porosity that may or may not be biodegradable at a predetermined rate.
(17) FIG. 6 shows an embodiment of implant 3 that includes a monitoring probe 6. Monitoring probe 6 may be incorporated into implant 3 at the time of manufacture or be attached to specially designed fixtures that allow probe 6 to be held in position such that probe 6 may be secured in direct contact with the underlying brain or associated structures by way of apertures within implant 3. Probe 6 may have one or numerous monitoring functions such as intracranial pressure, temperature, electroencephalometric, blood gas saturation, pH, and microdialysis for biochemical monitoring.
(18) FIG. 7 shows an embodiment of implant 3 that includes a therapeutic delivery mechanism or substance, such as slow release biodegradable substances 7 that release therapeutic agents in a predictable time released way.
(19) FIG. 8 shows an embodiment of implant 3 that includes an enclosed channel 8 which is accessible via a mechanism 9. Mechanism 9 may be an aperture and/or probe.
(20) FIG. 9 shows an embodiment of implant 3 that includes a network of channels 10. The network of channels 10 may allow closed circulation of fluid to and from an external pump.
(21) FIG. 10 shows an embodiment of implant 3 that includes a semi-permeable membrane 11. The semi-permeable membrane 11 may be used between channels 10 and the surface of a brain. The membrane may be designed so that only substances with specific molecular weights may cross.
(22) FIG. 11 shows an embodiment of implant 3 that includes a network of channels 12. The network of channels 12 may be connected to and from an incorporated port or reservoir 13. Such a port could be accessed percutaneously via injection or through access apertures so that therapeutic substances and stem cells could be introduced to promote the formation of new bone to integrate the invention with the surrounding skull.
(23) Throughout this specification and the claims that follow, unless the context requires otherwise the words comprise, comprises, comprising will be understood to mean the inclusion of the stated Integer, step or group of integers or steps but not the exclusion of any of other integer, step or group of integers or steps.
