초록 ▼

A disposable articulated spacing device for use as a temporary joint prosthesis includes a first member secured during an implantation procedure to a first articulation end and a separate and independent second member secured separately during the implantation procedure to the other articulation end

A disposable articulated spacing device for use as a temporary joint prosthesis includes a first member secured during an implantation procedure to a first articulation end and a separate and independent second member secured separately during the implantation procedure to the other articulation end, both members being pre-formed and made entirely of biological compatible and porous material suitable to be added with pharmaceutical and therapeutical products. The pre-formed members are reciprocally coupled in an articulated manner to maintain a suitable joint space and at least a partial articulation for the time necessary to perform the further implantation of a joint prosthesis.

대표청구항 ▼

The invention claimed is: 1. A method for treating joints of the human body, particularly for temporary replacing an explanted permanent joint prosthesis, comprising: providing a preformed disposable articulated spacing device including at least one pre-formed first member and at least one pre-form

The invention claimed is: 1. A method for treating joints of the human body, particularly for temporary replacing an explanted permanent joint prosthesis, comprising: providing a preformed disposable articulated spacing device including at least one pre-formed first member and at least one pre-formed second member both made entirely of biologically compatible and porous material, said first member and said second member being distinct bodies independent of and separate from one another, said first member and said second member having a porosity in their base material or suitable cavities formed on their outer surfaces adapted to be filled with pharmaceutical and therapeutical products in the form of liquid solutions, said first member and said second member being initially free of pharmaceutical and therapeutical products; adding pharmaceutical and therapeutical products in the form of liquid solutions to said first member and said second member either by direct contact and absorption or by insertion thereof in said suitable cavities; after the adding of said liquid solutions to said first member, inserting said first member into a patient and securing said first member to a first articulation end in the patient; after the adding of said liquid solutions to said second member, inserting said second member into the patient and securing said second member to a second articulation end in the patient, said second member being inserted into the patient separately from said first member and after the inserting of said first member; and reciprocally coupling said first member and said second member to one another in an articulated manner to maintain a suitable joint space and at least partial articulated mobility for the time necessary to perform the further implantation of a new permanent joint prosthesis. 2. Method according to claim 1, wherein said biologically compatible and porous material is selected from the group consisting of metals, metallic alloys, organo-metals, ceramics, glasses, plastics materials, bone cements and combinations thereof. 3. Method according to claim 2, wherein said plastics materials are selected from the group consisting of thermoplastic polymers, acrylic resins, polyethylene, polypropylene, and resins thermoformable by blow molding or injection molding. 4. Method according to claim 2, wherein said plastics materials are cold-formable resins. 5. Method according to claim 1, wherein said biologically compatible and porous material is a bone cement. 6. Method according to claim 1, wherein said pharmaceutical and therapeutical products are selected from the group consisting of active medical principals, antibiotics and radiopacifiers. 7. Method according to claim 1, wherein said first member and said second member are configured so as to allow a roto-translatory movement of condyles during a flexing/extending movement of a limb. 8. Method according to claim 7, wherein said first member and said second member have respective contact surfaces with a minimum coefficient of friction so as to allow a high degree of articular mobility. 9. Method according to claim 1, wherein said first member and said second member each have one of a plurality of predetermined different sizes adapted to fit patients or different size requirements. 10. Method according to claim 1, further comprising anchoring said first member and said second member to the articulation ends via anchoring means provided on said first member and said second member. 11. Method according to claim 10, wherein said anchoring means consist of respective projections or rod shaped distal portions. 12. Method according to claim 1, further comprising joining said first member and said second member to said joint ends with bone cement. 13. Method according to claim 1, wherein said first articulation and said second articulation are in a knee joint, said first member and said second member comprising a femoral member and a tibial member. 14. Method according to claim 13, wherein said femoral member consists of a first body substantially in the shape of a shell to reproduce femoral condyles and that said tibial member consists of a second body of substantially prismatic shape with predetermined thickness to replace a resected tibial flat portion. 15. Method according to claim 1, wherein said first member and said second member are rigid members. 16. Method according to claim 15, wherein said first member and said second member are of standard sizes. 17. Method according to claim 1, wherein the securing of said first member and said second member to said first articulation end and said second articulation end includes securing said first member and said second member in their respective preformed shapes to said first articulation end and said second articulation end. 18. A disposable articulated method for temporarily replacing an explanted permanent joint prosthesis, comprising: providing at least one preformed first member ane at least one preformed second member, said first member and said second member being independent of and separate from one another; inserting said at least one preformed first member into a patient and securing said at least one preformed first member to a first articulation end in the patient; and inserting said at least one preformed second member into the patient and securing said at least one preformed second member to a second articulation end in the patient, said at least one preformed second member being inserted into the patient separately from said at least one preformed first member and after the inserting of said at least one preformed first member, both said first member and said second member being made entirely of biological compatible and porous material suitable for receiving a pharmaceutical or therapeutic agent, reciprocally coupling said first member and said second member in an articulated manner to maintain a suitable joint spacing and at least partial articulated mobility for a time necessary to perform implantation of a new permanent joint prosthesis, said first member and said second member being initially free of pharmaceutical and therapeutic products, immediately prior to implantation of said first member and said second member in a patient, adding, to said first member and said second member, pharmaceutical and therapeutic agents in the form of liquid solutions, either by direct contact and absorption or by insertion thereof in suitable cavities of said first member and said second member.