Abstract: A novel method for utilizing an implant in a body of a patient includes placing within a cavity in the body of the patient an implant constructed of biocompatible and biodegradable material configured to support the tissue surrounding the cavity, the implant having radio-opaque properties; and directing a radiation beam to the implant.

Abstract: A method for utilizing an implant in a breast cavity in a human breast, comprising forming a substantially radio-opaque implant constructed of biodegradable material, the biodegradable material being elastic, compressible, expandable, and allowing for in-growth of fibrous tissue into the biodegradable material, the substantially radio-opaque implant being compressed during implantation in the breast cavity; and the substantially radio-opaque implant configured to expand in the breast cavity when implanted within the breast cavity for supporting the tissue surrounding the breast cavity.

Abstract: A method for utilizing an implant in a human breast includes forming a breast cavity within the breast at a lumpectomy site, the breast cavity having surrounding tissue; forming a substantially radio-opaque implant constructed of biocompatible and biodegradable material configured to allow for in-growth of fibrous tissue into and replacing the biocompatible and biodegradable material, the biocompatible and biodegradable material being elastically compressible; sizing the substantially radio-opaque implant to occupy the breast cavity; and implanting within the breast cavity the substantially radio-opaque implant to support the tissue surrounding the breast cavity, the step of implanting including compressing the biocompatible and biodegradable material.

Abstract: A method for utilizing an implant in a human breast includes forming a breast cavity within the breast at a lumpectomy site, the breast cavity having surrounding tissue; forming a substantially radio-opaque implant constructed of biocompatible and biodegradable material configured to allow for in-growth of fibrous tissue into and replacing the biocompatible and biodegradable material, the biocompatible and biodegradable material being elastically compressible; sizing the substantially radio-opaque implant to occupy the breast cavity; and implanting within the breast cavity the substantially radio-opaque implant to support the tissue surrounding the breast cavity, the step of implanting including compressing the biocompatible and biodegradable material.

Abstract: A method of partial breast radiation therapy includes placing within a breast cavity a substantially radio-opaque implant constructed of biocompatible material, said substantially radio-opaque implant supporting the tissue surrounding the breast cavity; and directing a radiation beam to said substantially radio-opaque implant serving as a target for delivery of radiation therapy to margins around the breast cavity, such that the radiation beam does not materially irradiate the whole of the breast.

Abstract: A method of partial breast radiation therapy includes placing within a breast cavity a substantially radio-opaque implant constructed of biocompatible material, said substantially radio-opaque implant supporting the tissue surrounding the breast cavity; and directing a radiation beam to said substantially radio-opaque implant serving as a target for delivery of radiation therapy to margins around the breast cavity, such that the radiation beam does not materially irradiate the whole of the breast.

Abstract: A novel method of partial breast radiation utilizing a breast implant which can provide a stable and improved target for stereotactic radiation treatment.

Abstract: A novel method of partial breast radiation utilizing a breast implant which can provide a stable and improved target for stereotactic radiation treatment.

Abstract: A surgical drape includes a first, closed container within which a first sheet is disposed. The first sheet has first and second opposed ends, the first end of the first sheet being removable from the container so as to remove a desired portion of the first sheet from the container, the second end of the first sheet remaining within the container. Preferably, the first container is laid across a desired portion of the table prior to placing the patient on the table. After the patient has been positioned properly and prepped, the first sheet can be pulled from underneath the patient and pulled out of the first container so that the sheet covers the table in the area of surgical interest and then covers the entire side or end of the table down to the floor. After the surgical procedure has been completed, the first sheet and the container can be removed and discarded.

Abstract: A carotid comfort control jacket keeps the wearer cool or warm during outside sporting events, for example. The jacket also can be used to enhance patient comfort during surgery or recovery. Treatment of various medical conditions can be carried out using the jacket. The jacket preferably is reusable and constructed of a waterproof inner lining and a soft outer cover. The outer cover can be made of various materials and in various colors. Filler caps or fittings are provided to fill the jacket inner liner with cooling fluid. Also included is a flow-through configuration.

Abstract: A surgical draping system (2), separates the sterile surgical field from the unsterile surgical table and isolates the patient so that sterile surgical procedures can be performed without chance of contamination. The components of the surgical draping system are provided folded and in sterile condition inside a sealed bag container. The sealed bag (4), is placed acres an operating table (8), prior to placement of the patient. Once the patient has been positioned on the operating table (8), the bag (4), is opened and the surgical drape (10), is extended. The draping system may include coverings for legs or arms and a top drape. The draping system isolates the operating field in a simple and sterile manner and can be discarded at the termination of the procedure.

Abstract: A surgical instrument organizer for holding surgical instruments on a horizontal surface includes an elongate strip having opposed front and rear walls, end walls, an upper portion, and a lower portion, and a support member in engagement with the strip, the support member in use maintaining the front and rear walls generally perpendicular to the horizontal surface. The upper portion is defined by a plurality of notches, the notches being of a size and shape to receive surgical instruments and maintain them in a propped-up, spaced-apart position. In the preferred embodiment, each of the notches is generally V-shaped, with each notch being about 0.875 inch deep and having side walls that terminate in points spaced about 0.375 inch from each other. Preferably the foam is made of crosslinked, closed-cell polyolefin. The support member can be provided in a variety of forms, including spaced stands, an elongate block, and an open-ended surgical tray.

Abstract: A tissue marking implant includes a matrix material and a dye marker. The implant, which can be formed entirely of bioresorbable material such as a collagen foam, is sized and shaped to replace excised tissue. The implant supports surrounding tissue upon implantation, while allowing for in-growth of fibrous tissue to replace the implant. According to various alternative embodiments, the implant is elastically compressible, or can be formed from self-expanding foam or sponges, and can be implanted through a cannula or by injection, as well as by open procedures. The implant can carry therapeutic and diagnostic substances. The dye marker leaches from the implant such that a surgeon, upon subsequent surgical intervention, visibly recognizes the tissue marked by the dye marker.

Abstract: A surgical drape includes a first, closed container within which a first sheet is disposed. The first sheet has first and second opposed ends, the first end of the first sheet being removable from the container so as to remove a desired portion of the first sheet from the container, the second end of the first sheet remaining within the container. Preferably, the first container is laid across a desired portion of the table prior to placing the patient on the table. After the patient has been positioned properly and prepped, the first sheet can be pulled from underneath the patient and pulled out of the first container so that the sheet covers the table in the area of surgical interest and then covers the entire side or end of the table down to the floor. After the surgical procedure has been completed, the first sheet and the container can be removed and discarded.

Abstract: A medical-electronic body fluid accounting system for use in surgical procedures and in post-operative and non-surgical care to afford a running account of the fluid intake to a patient and fluid outtake therefrom. The system is provided with a microcomputer to which is applied digital data derived from a plurality of fluid input source channels and fluid output source channels which together represent the prevailing fluid input and output sources associated with the patient. Included in the input source channels are those monitoring the flow of fluids being fed intraveneously into the patient, each such input channel having a sensor which generates a signal representing the volume of a particular fluid, such as a saline solution, being infused into the patient, this signal being converted into a corresponding digital value.