Tissue marking implant
A method for marking a surgically formed cavity in a patient includes providing an implant comprising a matrix material and a marking material, the matrix material configured to be elastically compressible; modifying the shape and size of the implant to fit the shape and size of the surgically formed cavity in the patient, the implant being configured to fill the surgically formed cavity and support tissue surrounding the surgically formed cavity and to allow in-growth of fibrous tissue into and replace at least a portion of the matrix material; and inserting the implant into the surgically formed cavity.
1. A method for marking a surgically formed cavity in a patient, comprising:
providing an implant comprising a matrix material and a marking material, the matrix material configured to be elastically compressible;
modifying the shape and size of the implant to fit the shape and size of the surgically formed cavity in the patient, the implant being configured to fill the surgically formed cavity and support tissue surrounding the surgically formed cavity and to allow in-growth of fibrous tissue into and replace at least a portion of the matrix material; and
inserting the implant into the surgically formed cavity.
2. The method of claim 1 , comprising inserting a dye into the matrix material.
3. The method of claim 1 , wherein the matrix material comprises one of a foam or sponge, and is at least partially resorbable.
4. The method of claim 1 , wherein the matrix material comprises a foamed bioabsorbable protein.
5. The method of claim 1 , wherein the matrix material comprises of a foamed collagen.
6. The method of claim 1 , comprising inserting at least one medicinal, therapeutic, or diagnostic substance into the matrix material.
7. The method of claim 6 , wherein the at least one medicinal, therapeutic, or diagnostic substance is selected from the group consisting of radiation materials, antibiotics, chemotherapies, cancer therapeutics, hemostatic materials, hormone therapeutics, and radiographic markers.
8. The method of claim 1 , comprising surrounding the matrix material with a shell.
9. The method of claim 8 , wherein the shell comprises a compressed matrix material.
10. A method for forming an implant for marking a surgically formed cavity in a patient, comprising:
providing a matrix material and a marking material to form an implant, the matrix material configured to be elastically compressible; and
modifying the shape and size of the implant to fit the shape and size of the surgically formed cavity in the patient, the implant being configured to fill the surgically formed cavity and support tissue surrounding the surgically formed cavity and to allow in-growth of fibrous tissue into and replace at least a portion of the matrix material.
11. The method of claim 10 , comprising inserting a dye into the matrix material.
12. The method of claim 10 , wherein the matrix material comprises one of a foam or sponge, and is at least partially resorbable.
13. The method of claim 10 , wherein the matrix material comprises a foamed bioabsorbable protein.
14. The method of claim 10 , wherein the matrix material comprises of a foamed collagen.
15. The method of claim 10 , comprising inserting at least one medicinal, therapeutic, or diagnostic substance into the matrix material.
16. The method of claim 15 , wherein the at least one medicinal, therapeutic, or diagnostic substance is selected from the group consisting of radiation materials, antibiotics, chemotherapies, cancer therapeutics, hemostatic materials, hormone therapeutics, and radiographic markers.
17. The method of claim 10 , comprising surrounding the matrix material with a shell.
18. The method of claim 17 , wherein the shell comprises a compressed matrix material.
19. A method of operating a marker delivery device for marking a surgically formed cavity in a patient, comprising:
providing a delivery cannula having a distal discharge opening;
providing an implant comprising a matrix material and a marking material, the matrix material being configured to be elastically compressible and configured to allow in-growth of fibrous tissue into and replace at least a portion of the matrix material after implantation in the surgically formed cavity;
forming the implant to a shape and a size of the surgically formed cavity to fill the surgically formed cavity and support tissue surrounding the surgically formed cavity;
compressing the implant to fit within the delivery cannula;
inserting the delivery cannula into the patient until the distal discharge opening of the delivery cannula is located within the surgically formed cavity; and
discharging the implant from the delivery cannula through the distal discharge opening, wherein the matrix material expands such that the implant fills the surgically formed cavity.
20. The method of claim 19 , comprising surrounding the matrix material with a shell.