The present application relates to the glenoid implant surgery using patient specific instrumentation or like assistance devices.
In orthopedic shoulder surgery, implant components are installed on the glenoid portion of the scapula (i.e., shoulder blade) and/or on the humerus, to replicate the shoulder joint. When an implant is installed on the scapula, it is commonly installed in the glenoid cavity, also known as the glenoid or glenoid fossa. The glenoid is a cavity that receives the head of the humerus in an anatomical shoulder. When an implant is used with the glenoid, the base of the implant is located within the glenoid, and could be secured thereto by fasteners such as screws, or using cement and/or fixation peg or keel.
One of the challenges in the case of shoulder surgery is with the placement of a glenosphere. Indeed, an improperly placed glenosphere could impact natural movements of the arm relative to the shoulder and require a premature revision surgery. On the other hand, there exists difficulty with the positioning of the glenosphere due to its hemispherical shape. It would be desirable to provide assistance in the positioning of the glenosphere.
Patient specific instrumentation (hereinafter “PSI”) pertains to the creation of instruments that are made specifically for the patient. PSI are typically manufactured from data using imagery to model bone geometry. Therefore, PSI have surfaces that may contact the bone in a predictable way as such contact surfaces are specifically manufactured to match the surface of a bone. It would therefore be desirable to use PSI technology in shoulder surgery.
It is therefore an aim of the present invention to provide a patient specific glenosphere implant positioning device for assisting in implant the glenosphere implant.
Therefore, in accordance with a first embodiment of the present disclosure, there is provided a glenosphere-implant positioning device comprising: a coupling body having at least a first portion adapted to contact a spherical portion of a glenosphere implant, and a second portion adapted to contact an underside portion of the glenosphere implant, such that the coupling body is configured to be releasably coupled to a glenosphere implant in a known manner; and a guide connected to the coupling body and configured to be slidingly engaged to a guide pin representative of a desired implanting orientation of the glenosphere implant or to a periphery of an implanted baseplate.
Further in accordance with the first embodiment, wherein the coupling body has a C shape.
Still further in accordance with the first embodiment, the first portion of coupling body is an arcuate member having an inward sphere-matching surface configured to conformly contact the spherical portion of a glenosphere implant.
Still further in accordance with the first embodiment, the second portion is a flange projecting inwardly from an edge of the arcuate member.
Still further in accordance with the first embodiment, the guide is an edge surface of the flange configured to form a sliding joint with the periphery of the implanted baseplate.
Still further in accordance with the first embodiment, the C shape is configured to be releasably coupled over more than 180 degrees of the glenosphere implant.
Still further in accordance with the first embodiment, the guide defines a channel configured to be slidingly engaged to a guide pin, the glenosphere-implant positioning device further comprising a patient specific geometry between the coupling body and the channel based on a planned position and orientation between the guide pin and a baseplate upon which the glenosphere implant is to be implanted.
Still further in accordance with the first embodiment, at least one connector projects from the coupling body and configured for releasable engagement with an impactor tool interface contacting the glenosphere-implant.
Still further in accordance with the first embodiment, the at least one connector is configured to align the impact tool portion with the desired implanting orientation.
Still further in accordance with the first embodiment, the glenosphere-implant positioning device is a monolithic component.
In accordance with a second embodiment of the present disclosure, there is provided a kit comprising: the glenosphere-implant positioning device as described above; the baseplate configured to be anchored to a bone; and the glenosphere implant for mating engagement with the baseplate, the glenosphere implant configured to be releasably coupled to the glenosphere-implant positioning device in a known manner.
Further in accordance with the second embodiment, an impactor tool interface is adapted to be positioned directly against a surface of the glenosphere implant.
Still further in accordance with the second embodiment, the impactor tool interface is adapted to be releasably connected to the glenosphere-implant positioning device such that an axis of an impactor tool is parallel to a normal to a plane of the baseplate.
In accordance with a third embodiment, there is provided a method for installing a glenosphere implant on an implanted baseplate, comprising: releasably coupling the glenosphere implant to glenosphere-implant positioning device; forming a translational joint between the glenosphere-implant positioning device and one of a guide pin and the baseplate, the translational joint being in a fixed desired orientation relative to the implanted baseplate; moving the glenosphere implant releasably coupled to glenosphere-implant positioning device along the fixed desired orientation into engagement with the baseplate; and impacting the glenosphere implant onto the baseplate along the fixed desired orientation.
Further in accordance with the third embodiment, forming a translational joint comprises sliding a guide channel of the glenosphere-implant positioning device onto the guide pin.
Still further in accordance with the third embodiment, forming a translational joint comprises for adding a rotational degree of freedom to the translation joint.
Still further in accordance with the third embodiment, forming a translational joint comprises displacing an edge surface of the glenosphere-implant positioning device into engagement with a circumferential surface of the implanted baseplate.
Still further in accordance with the third embodiment, further comprising releasably connecting an impactor tool portion to the glenosphere-implant positioning device and against the glenosphere implant prior to impacting.
Still further in accordance with the third embodiment, releasably connecting an impactor tool portion comprises aligning the impactor tool portion with the fixed desired orientation.
Still further in accordance with the third embodiment, wherein releasably coupling the glenosphere implant to glenosphere-implant positioning device comprises elastically deforming the glenosphere-implant positioning device during coupling.
Referring to the drawings and more particularly to
The positioning device 10 has a coupling body 12 designed to be releasably coupled to the glenosphere implant A, in a known manner, such that a position of an axis of the glenosphere implant A (for instance a normal to a plane of its underside) is known relative to the coupling body 12. The positioning device 10 further comprises a guide 14. The guide 14 has a channel 16 that is slidably mountable on the guide pin C. Therefore, the assembly of the guide pin C and guide 14 forms a translational joint along the guide pin C, i.e., along a longitudinal axis of the guide pin C. Moreover, when the guide pin C has a circular section as in
The positioning device 10 may be said to be patient specific, in that the size of the coupling body 12, and/or the distance and orientation between the coupling body 12 and the channel 16 may result from patient specific data obtained preoperatively or intraoperatively, for example as in described in the above-referred PCT application. Stated differently, the position and orientation of the guide pin C relative to the baseplate B has been planned and replicates the planning, and the positioning device 10 is created as a function of the planned relation between the baseplate B and guide pin C.
As shown in
Referring to
The assembly may be moved further along the guide pin C and rotated until the implant A is substantially aligned with the baseplate B. The complementary coupling between the implant A and the baseplate B will assist the operator in finding the appropriate alignment, and the constraints of the translation joint—i.e., the guide 14 on the guide pin C—will preserve the desired orientation of the implant A relative to the baseplate B. Hence, the guide pin C ensures that the axis of the implant A is oriented as planned relative to the baseplate B.
Once this achieved, the implant A may be secured to the baseplate B, for instance by impacting. As shown in
According to another embodiment shown in
Connectors 23 may be provided on a top end of the coupling body 12. The connectors 23 are sized for receiving therebetween the end of the impactor tool, such as the impactor tool interface D. These connectors 23 may further assist in preserving the desired orientation of the implant A relative to the baseplate B, for instance by aligning the shaft of the impactor tool with the guide pin C, for visual assistance, and thus with the normal of the baseplate plane B1. The guide channel 14 may be formed in one of the connectors 23. The guide channel 14 may be laterally slotted to facilitate removal, although it is contemplated to suggest removal of the guide pin C prior to uncoupling the positioning device 10/10′ from the implant A installed in the baseplate B.
A block 24 also projects upwardly from the coupling body 12. The block 24 has a threaded hole 25 for being connected to a rod of a manipulating tool. As observed in
The coupling body 12 may have any appropriate shape to be coupled to the implant A. As the implant A has a hemispherical surface, the coupling body 12 may have sphere-matching surfaces.
Although patient specific technology is suggested above, it is also considered to use a standard positioning device 10 (i.e., non-patient specific). In such a case, the device 10 would be attached to a trial version of the glenosphere that could easily be inserted on the baseplate. A pin could be driven through the superior hole of the device 10, for subsequent use to insert the permanent glenosphere implant A. As yet another embodiment, the positioning and orienting of the guide pin C could be navigated, for subsequent use of a standard positioning device 10.
According to another embodiment shown in
Referring to
A block 31 also projects upwardly from the coupling body 12 of the positioning device 10″. The block 31 may be used with pliers or other tool, for removal of the positioning device 10″ from the implant A once assembled to the baseplate B. Although not shown, it is considered to provide connectors for impactor tool D, and threaded hole 25 in the block 31. To releasably couple the positioning device 10″ to the glenosphere implant A, the positioning device 10″ is made of a material capable of elastic deformation when deformed to be coupled to the glenosphere implant A, such a medical-grade polymer or metal. In an embodiment, the positioning device 10″ is a monolithic component. However, the rigidity and structural integrity of the positioning device 10″, as the inward flange 22 must keep its shape for the joint edge surface 30 to form a reliable joint with the circumferential surface B2 of the baseplate B.
The method described above with reference to
The positioning device 10/10′/10″ may be provided as an installation kit with at least the glenosphere implant A, and possibly with the baseplate B, guide pin C and impactor tool interface D, along with other tools such as fasteners, etc.
The present application claims priority of U.S. Provisional Application No. 62/138,175, filed on Mar. 25, 2015 and on U.S. Provisional Application No. 62/138,746, filed on Mar. 26, 2015 and incorporated herein by reference.
Number | Date | Country | |
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62138175 | Mar 2015 | US | |
62138746 | Mar 2015 | US |