US20110166661A1

US20110166661A1 - Apparatus for fitting a shoulder prosthesis

Info

Publication number: US20110166661A1
Application number: US13/007,355
Authority: US
Inventors: Pascal Boileau; Gilles Walch; Irene Gosset; Pierric Deransart
Original assignee: Tornier SAS
Current assignee: Tornier SAS
Priority date: 2007-01-30
Filing date: 2011-01-14
Publication date: 2011-07-07
Also published as: US20190358045A1; US20170042687A1; US10251755B2; FR2911773B1; US8864834B2; EP1952788A1; EP1952788B1; WO2012095747A1; US11185417B2; EP3335676A1; US20150012104A1; JP5405753B2; FR2911773A1; EP1952771B1; US10413416B2; US20080183297A1; EP1952771A1; JP2008183412A

Abstract

Method and set of surgical instruments for fitting a shoulder prosthesis, and the shoulder prosthesis. The proposed method seeks to interpose a bone graft between the previously prepared glenoid surface of a scapula of a patient's shoulder and the face of a glenoid prosthetic component opposite the articular surface. The set of instruments permit the bone graft to be taken from the upper epiphysis of the humerus, either in situ or ex vivo.

Description

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a continuation-in-part application of U.S. patent application Ser. No. 12/020,913 filed Jan. 28, 2008, entitled “Method and Apparatus for Fitting a Shoulder Prosthesis,” which claims priority to French Application No. 0700622, entitled “Méthode et ensemble d'instrumentation chirurgicale pour poser une prothèse totale d'épaule inversée, et prothèse correspondante,” filed Jan. 30, 2007 and also claims the benefit of U.S. Provisional Application Ser. Nos. 60/888,437 filed Feb. 6, 2007, 60/971,762 filed Sep. 12, 2007 (both entitled “Method and Apparatus for Fitting an Inverted Shoulder Prosthesis”) and U.S. Provisional Application Ser. No. 61/015,042, entitled “Intra-Articular Joint Replacement,” filed Dec. 19, 2007, the complete disclosures of each of which are hereby incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to an inverted or an anatomical shoulder prosthesis including a graft to lateralize a glenoid component of the shoulder prosthesis.

BACKGROUND OF THE INVENTION

Total shoulder prostheses, are commonly said to be inverted when they comprise, on the one hand, a glenoid part integral with the glenoid surface of a scapula of a patient's shoulder and delimiting a convex articular surface and, on the other hand, a humeral part integral with the humerus of the shoulder and delimiting a concave articular surface, the cooperation of these articular surfaces allowing an articulated connection to be reproduced at the shoulder. With this type of prosthesis, it is common, during adduction movement of the shoulder, for the lower portion of the humeral prosthetic part to strike the pillar of the scapula, i.e. the lower portion of the bone glenoid surface located, when the patient stands upright, just below the glenoid prosthetic part. This interference between the humeral prosthetic part and the scapula limits the range of the adduction movement and may cause pain to the patient or even lead to the prosthesis becoming dislodged, in particular by osteolysis of the scapula.

BRIEF SUMMARY OF THE INVENTION

Various aspects of the invention relate to surgical methods and corresponding surgical instruments for reducing risk of interference between the scapula and the humeral part of an inverted or an anatomical shoulder prosthesis. All references to a “shoulder prosthesis” should be interpreted to include a total shoulder prosthesis with a humeral component and a glenoid component (including anatomical, inverted, or interpositional configurations), or a partial shoulder prosthesis with a glenoid component with an anatomical or resurface humeral head.
Some embodiments relate to a surgical method for fitting an inverted shoulder prosthesis, the prosthesis including a glenoid component having a convex articular surface and an opposing face, this fitting method including successive preoperative steps in which a graft is provided, the graft is placed on the previously prepared glenoid surface of a scapula of a patient's shoulder, and the glenoid component is implanted so as to cover the graft positioned on the glenoid surface with the opposing face of the glenoid component and to anchor the glenoid component in the glenoid surface through the graft. In some embodiments, a geometric center of articulation of the glenoid component is situated at the bone face in the glenoid surface, where a radius of curvature of a convex articular surface of the glenoid component is selected so a center of rotation of the glenoid component is in or behind a plane comprising a distal surface of the graft.
In some embodiments, the method includes “lateralizing” the glenoid component relative to the patient's scapula, withdrawing the glenoid component from the patient's scapula in a plane frontal to the patient, by interposing the graft between this glenoid component and the glenoid surface. In other words, the graft forms an outer lateral extension of the glenoid surface, extending the scapula, whereas the combination of the graft and the prosthetic glenoid component forms a composite prosthetic unit. The glenoid component is optionally implanted so as to cover a side of the graft opposing the glenoid surface, where the component includes a bone anchoring structure or anchor portion, such as a central tail, sufficiently elongate to pass through the graft and in the bone of the scapula delimiting the glenoid surface. According to some embodiments, once the graft has fused with the glenoid surface, a distal surface of the graft becomes the effective glenoid surface. References to glenoid surface should be interpreted to include a prepared or an unprepared exposed surface of a glenoid cavity.
In some embodiments, an articular face of the glenoid component occupies, relative to the scapula, a position laterally more remote than a position the articular face would occupy were the graft omitted. Removing the glenoid component laterally helps reduce risk of interference between the pillar of the scapula and the lower portion of the humeral prosthetic part cooperating with the glenoid articular face. The lateralization of the prosthetic glenoid component also helps increase tension in the rotator muscles of the shoulder and the co-adaptation vector of the deltoid muscle, which helps stabilize the prosthetic glenoid and humeral components and promote better mobility in relative rotation with a lower risk of shoulder dislocation. Furthermore, compared to typical inverted shoulder prostheses, which can be described as a medialized prostheses, lateralized prostheses according to various embodiments help restore some of the curved surface of the patient's shoulder, giving the shoulder a more pleasing appearance than the “coat hanger” appearance conferred by medialized prostheses.
Some embodiments relate to glenoid components that include adjustable length tails, or anchoring structures for use with grafts having a variety of thicknesses, according to embodiments of the present invention. For example, in some embodiments, a surgeon or other user selects a desired bone graft thickness and adjusts the overall length of an anchoring portion of the glenoid component for use with that graft thickness. By adjusting the overall length of the anchoring structures, the glenoid components are better able to facilitate lateralization of the center of rotation of the glenoid component with a secure affixation into the boney structure forming the glenoid, for example, as well as additional or alternative advantages.
According to various embodiments, complete exposure of the glenoid surface is not required and is optionally limited to positioning of the graft, promoting efficiency and reproducibility. The graft is optionally taken from the patient, although allografts, xenografts, metals, natural or synthetic materials are employed as desired. In some embodiments, the graft is taken from the upper epiphysis of the humerus of the patient's shoulder, such that the graft originates from the patient, thereby helping to limit risk of rejection, poor biological compatibility, and transmission of disease or infection, for example. Moreover, efficiencies are realized in that often times in order to implant a corresponding humeral component, the epiphysis of the patient's humerus is to be prepared by withdrawing a substantial amount of cancellous bone matter from this epiphysis which can then be used to provide the graft rather than, for example, simply discarding such bone matter. Accordingly, in some embodiments, the method includes a shaping step in which the bone matter forming the upper humeral epiphysis is shaped into a one-piece volume extending in length about an axis inclined relative to the longitudinal direction of the humerus, and a cutting step in which the volume of bone matter is removed from the humerus by cutting the humeral epiphysis transversely to the axis of this volume, the volume of bone matter thus removed forming the graft.
According to some methods, a surgical joint repair includes adjusting a length of the graft along an axis of a volume of bone matter and shaping respective longitudinal end faces of the graft to be substantially complementary to an opposing face of the glenoid component and the glenoid surface previously prepared. During the shaping step, the shaped volume of bone matter is chosen from a cylinder and a frustum of a cone, for example, centered on the axis of the shaped volume of bone matter. Before or during the shaping step, the end of the upper humeral epiphysis is resected as desired, for example, over a first plane. During the cutting step, the humeral epiphysis is optionally cut over a second plane, the first and second planes being transverse to the axis of the shaped volume of bone matter. A relative inclination of the first and second planes is adjusted as desired. During or after the shaping step, a recess is optionally formed that is centered on the axis of the volume of bone matter in the humeral epiphysis. In some embodiments, the glenoid component is anchored in the glenoid surface through the recess and, before carrying out the shaping step, a marker pin is inserted into the humeral epiphysis, thereby allowing, during the shaping step, positioning of the axis of the volume of bone matter relative to the humerus.
According to some other embodiments, rather than taking the graft from the patient's humeral epiphysis, the graft is taken from a bone region in the patient other than the upper humeral epiphysis, such as the patient's ilium, or the graft is formed as an allograft, a graft of synthetic origin, a graft of metallic origin, combinations thereof, or other material. For example, in some embodiments a protection layer is attached to at least a part of the graft that is not in contact with the glenoid surface and at least a part of the opposing face of the glenoid component is supported on the protection layer. In some embodiments, some or all of the surfaces on the glenoid component that engage with the graft are covered with hydroxyapatite or materials having a functionally similar surface state, such as a honeycomb surface state, allowing bone adhesion and rehabilitation to be improved. Selected surfaces of the glenoid component may be constructed of materials that facilitate fusion with bone, such as those disclosed in U.S. Pat. No. 7,250,550.
According to still other embodiments, the graft includes a purée of bone substance (e.g, originating from the patient, in such as from the upper epiphysis of the humerus, or from another, source, such as a synthetic or metallic source). In some embodiments, the purée of bone substance is advantageously used with a protective structure, such as a lattice shaped into a cage that is filled with the purée. The lattice cage optionally facilitates good exchange of biological flows between the purée forming the graft and the surrounding tissues of the shoulder.
The invention also relates to a set of surgical instruments for fitting a shoulder prosthesis. The set includes a shaping ancillary instrument that shapes the bone matter forming the upper humeral epiphysis of a humerus into a one-piece volume extending in length about an axis inclined relative to the longitudinal direction of the humerus, and a cutting ancillary instrument that cuts the humeral epiphysis shaped by the shaping ancillary instrument, for cutting the volume of bone matter transversely to the axis of this volume. The cutting ancillary instrument is optionally used to remove the volume of bone matter from the humerus that is formed into a graft.
The set of instruments according to the invention allows implementation of the fitting method defined hereinbefore, the shaping and cutting steps of which are respectively carried out by the shaping and cutting ancillary instrument. The volume of bone matter removed from the humerus using the cutting ancillary instrument can thus be used as the bone graft for carrying out the general fitting method defined hereinbefore in order laterally to offset the convex articular surface of a glenoid component of the prosthesis relative to the scapula of the patient's shoulder, during implantation of this glenoid component.
According to advantageous features of this set of instruments, taken in isolation or in any technically feasible combination:
the set comprises a resecting instrument for resecting the end of the humeral epiphysis, which resecting instrument is either carried by a specific resection ancillary instrument, distinct from the other ancillary instrument of the set or integrated in the shaping ancillary instrument;
the resecting instrument comprises a planar reamer so as to resect the humeral epiphysis over a first plane transverse to the axis of the volume of bone matter;
the set comprises a humeral epiphysis drilling instrument which is adapted to form a recess, centered on the axis of the volume of bone matter, in the humeral epiphysis and which is either integrated in the shaping ancillary instrument, or the resection ancillary instrument, or is carried by a specific drilling ancillary instrument distinct from the other ancillary instrument of the set;
the set comprises a marker pin or a similar marker instrument capable of being inserted into the humeral epiphysis and suitable for guiding the shaping ancillary instrument and optionally at least one of the other ancillary instrument of the set;
the set comprises an inserting ancillary instrument for inserting the marker pin into the humeral epiphysis, which inserting instrument is suitable for adjusting the direction of insertion of this pin relative to the humerus;
the inserting ancillary instrument comprises, on the one hand, a rounded bell-shaped body configured internally to cover the upper humeral epiphysis in the manner of a cap and, on the other hand, a guide for applying the marker pin, which guide opens into the body;
the shaping ancillary instrument comprises a bell-shaped saw which is suitable for cutting the bone matter forming the humeral epiphysis by shaping it into the volume of bone matter;
the saw has an optionally perforated cylindrical or frustoconical inner face so as to provide the volume of bone matter with the overall shape of a cylinder or frustum of a cone, centered on the axis of this volume;
the cutting ancillary instrument comprises a tubular block suitable for being slipped about the volume of bone mass shaped by the shaping ancillary instrument, this block delimiting, at its longitudinal end turned during operation toward the humerus, an incision zone in the humeral epiphysis, in order to cut the volume of bone matter transversely to the axis thereof;
the incision zone forms a transverse slot for the passage of a saw blade or the like, in order to cut the volume of bone matter over a second plane transverse to the axis of this volume; and
the cutting ancillary instrument comprises an annular body adapted to be mounted around the humeral epiphysis while surrounding at least the volume of bone matter shaped by the shaping ancillary instrument, this body delimiting a guide surface for a cutting instrument to cut at least the volume of bone matter transversely to its axis.
The invention also relates to an inverted shoulder prosthesis comprising a glenoid component having a convex articular surface and an opposing face, wherein the prosthesis comprises a protection layer for protecting a graft interposed, when the prosthesis is fitted, between said opposing face and the glenoid surface of a scapula of a patient's shoulder, this protection layer being suitable for both covering at least a part of the graft that is not in contact with the glenoid surface and forming a support for at least a part of said opposing face.
The graft protected by the protection layer of the prosthesis according to the invention can be taken from the upper humeral epiphysis using the set of instruments defined hereinbefore, or else be chosen from a graft taken from a bone region in the patient other than the upper humeral epiphysis, in particular from the patient's ilium, an allograft and a graft of synthetic or metallic origin. In practice, this prosthesis is fitted in accordance with the general method defined hereinbefore.
According to advantageous features of this prosthesis, the prosthesis optionally includes a protection layer, such as for example, a layer of hydroxyapatite or other material that has a functionally similar surface state, such as a honeycomb surface state, allowing bone adhesion and rehabilitation to be improved. In another embodiment, the protection layer includes a shape of a ring suitable for surrounding, in a close-fitting manner, the portion of the bone graft not in contact with the glenoid surface, it being appreciated that, in practice, this ring is used for a one-piece graft obtained, in particular, by the set of instruments as defined hereinbefore. The protection layer may also be a lattice shaped as a cage adapted to be filled with a purée of bone matter forming the graft.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING

A better understanding of the invention will be facilitated on reading the following description given merely by way of example and with reference to the drawings, in which:

FIG. 1 is a basic schematic illustration of an inverted shoulder prosthesis, implanted at a patient's shoulder;

FIG. 2 is a schematic elevation of an ancillary instrument of a set of instruments according to the invention, used in order to fit the prosthesis of FIG. 1;

FIG. 3 is a view similar to FIG. 2, illustrating another ancillary instrument pertaining to the set of instruments, to be applied to the patient's humerus after use of the ancillary instrument of FIG. 2;

FIG. 4 is a schematic perspective view of a further ancillary instrument pertaining to the set of instruments;

FIG. 5 is a view similar to FIG. 2, illustrating the humerus after use of the ancillary instrument of FIGS. 3 and 4;

FIG. 6 is a schematic perspective view of another ancillary instrument pertaining to the set of instruments;

FIG. 7 is a view similar to FIG. 2, illustrating the application of the ancillary instrument of FIG. 6 to the humerus after use of the ancillary instrument of FIG. 4;

FIGS. 8-12 show a second embodiment of a set of instruments according to the invention,

FIGS. 8, 9, 11 and 12 being similar respective schematic elevations of four ancillary instruments pertaining to this set and used in succession, to fit the prosthesis from FIG. 1, whereas

FIG. 10 is a partial perspective view of the ancillary instruments from FIG. 9, shown alone;

FIG. 13 is a basic schematic illustration of the glenoid part of an inverted shoulder prosthesis according to the invention;

FIG. 14 is a view similar to FIG. 13 of a variation of the prosthesis according to the invention;

FIGS. 15-21 illustrate various uses of a graft to lateralize the glenoid component of an inverted shoulder prosthesis according to an embodiment of the present invention;

FIGS. 22-26 illustrate various uses of a graft to lateralize the glenoid component of an anatomical shoulder prosthesis according to an embodiment of the present invention;

FIGS. 27-29 illustrate various uses of a graft to lateralize the glenoid component of an inverted shoulder prosthesis according to an embodiment of the present invention; and

FIGS. 30A-30F illustrate a method and tool set for preparing a graft in accordance with an embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

FIG. 1 shows a shoulder prosthesis 1 comprising a glenoid component 10 and a humeral component 20, respectively implanted in the scapula S and the humerus H of a patient's shoulder. The glenoid components shown herein are illustrated schematically. The method and apparatus of the various embodiments disclosed herein may be used with a variety of other glenoid components, such as for example those disclosed in U.S. Pat. Nos. 7,033,396; 6,953,478; 6,761,740; 6,626,946; 5,702,447 and U.S. Publication Nos. 2004/0220673; 2005/0278030; 2005/0278031; 2005/0278032; 2006/0020344, which are hereby incorporated by reference.
The glenoid component 10 comprises a head 11, also described as a head structure, which has, on the side opposing the glenoid surface G of the scapula S, a convex articular surface 11A, also described as a face, of generally hemispherical shape and, on the side turned toward the glenoid surface, an opposing face 11B. In the example considered in the figures, this face 11B is generally planar but, in non-illustrated variations, this face 11B can have a more elaborate geometry, being, for example, substantially concave or convex.
The glenoid component 10 also comprises an anchoring tail 12, also described as an anchor portion, which extends transversely so as to protrude from the face 11B, in the direction opposing the face 11A, and the free end part of which is securely anchored in the glenoid surface G, thus joining the glenoid component to the scapula S. In practice, in a manner not shown, the anchoring tail 12 can be provided, at its end turned toward the head 11, with a base accommodated inside the head 11, being securely joined thereto. In other words, more generally, the connection between the tail 12 and the head 11 can assume a broad range of forms, such as material continuity, respective wedging surfaces, attached mechanical assembly structures, etc. Also by way of non-illustrated variation, the tail 12 can be externally threaded or, generally, have a surface state promoting the anchoring thereof.
Between the face 11B of the glenoid head 11 and the glenoid surface G of the scapula S there is interposed a graft 2 having a substantially cylindrical outer shape with a circular base, the external diameter of which is substantially equal to that of the head 11. The outer lateral face 2A of the graft 2 thus extends substantially in the extension of the hemispherical face 11A. The graft 2 has, on its side opposing the glenoid surface G, a longitudinal end face or distal surface 2B covered by the face 11B of the head 11 and, on its side directed toward the glenoid surface, a longitudinal end face or medial surface 2C resting against the glenoid surface G. Once the graft 2 fuses with the glenoid surface G, the effective glenoid surface G is displaced laterally outward to the distal surface 2B of the graft 2.
In the example considered in the figures, the longitudinal end faces 2B and 2C are planar; this has proven to be an embodiment that is simple to handle and easy to obtain, as will be referred to hereinafter. However, in practice, these faces 2B and 2C can have more elaborate geometries: on one side, the face 2B is provided to be covered in a substantially complementary manner with the face 11B of the head 11, including in this face 11B the zones or the structure for connecting to the tail 12, it being understood that, as indicated hereinbefore, this face 11B can be generally concave, convex or planar; on the opposing side, the face 2C is provided to embrace the surface of the glenoid surface G, which has been previously prepared for this purpose, so that the face 2C and the glenoid surface G are substantially complementary and can equally well be planar or curved.
The graft 2 can be a one-piece bone graft, a plurality of random or pre-formed bone pieces, one or more layers of bone material, a purée of bone substance, or combinations thereof. In addition to the patient's bone, the graft 2 can also be formed from an allograft, a xenograft, a synthetic material, a porous metal or a combination thereof. The graft 2 can optionally be resorbable. The graft 2 may be used alone or in combination with bone replacements, bone fillers, bone cements and/or bone adhesives. Various bone replacements, bone fillers, bone cements and bone adhesives are disclosed in U.S. Pat. No. 6,692,563 (Zimmerman), which is hereby incorporated by reference. Various additives can be included in the graft 2, such as for example, bone growth agents or pain inhibitors. In one embodiment, reinforcing fibers are added to the purée of bone substance.
In some embodiments, the graft is formed of materials into which native bone will grow to create a structure with properties comparable to native bone, such as for example, a three-dimensional porous matrix or scaffold. Examples of a porous matrix or scaffold include a reticulated bioceramic framework, structured porous tantalum, synthetic fiber mesh, and the like. Various porous matrices and scaffoldings are disclosed in U.S. Pat. Nos. 4,479,271; 6,511,511; 6,605,117; 6,797,006; 6,902,584; and 7,250,550, which are hereby incorporated by reference.
The graft 2 can be made from a variety of synthetic compounds, such as for example, polyglycolide, polylactides, polycaprolactones, polytrimethylenecarbonates, polyhydroxybutyrates, polyhydroxyvalerates, polydioxanones, polyorthoesters, polycarbonates, polytyrosinecarbonates, polyorthocarbonates, polyalkylene oxalates, polyalkylene succinates, poly(malic acid), poly(maleic anhydride), polypeptides, polydepsipeptides, polyvinylalcohol, polyesteramides, polyamides, polyanhydrides, polyurethanes, polyphosphazenes, polycyanoacrylates, polyfumarates, poly(amino acids), modified polysaccharides (e.g., cellulose, starch, dextran, chitin, chitosan, etc.), modified proteins (e.g., collagen, casein, fibrin, etc.) and their copolymers, or combinations thereof. Other polymers include polyglycolide, poly(L-lactide-co-glycolide), poly(D,L-lactide-co-glycolide), poly(L-lactide), poly(D,L-lactide), poly(L-lactide-co-D,L-lactide), polycaprolactone, poly(L-lactide-co-caprolactone), poly(D,L-lactide-co-caprolactone) polytrimethylenecarbonate, poly(L-lactide-co-trimethylenecarbonate), poly(D,L-lactide-co-trimethylen-ecarbonate), polydioxanone and copolymers, and polymer blends thereof. Various methods of manufacturing the bone graft from a synthetic compound can be found in U.S. Pat. Nos. 6,767,928; 6,730,252; 6,541,022; 6,454,811, which are hereby incorporated by reference. Optionally, before or during the surgical procedure the graft 2 can be secured to the glenoid component 10 using additional methods known in the art, such as for example biocompatible adhesives, mechanical fasteners, or combinations thereof.
The graft 2 can be made from a variety of metallic solutions, such as for example, a highly porous metal having interconnecting pores. In one embodiment, the porous metal is about 80% porous. The metal has a porosity giving it a mechanical and physical structure similar to that of bone such that bone ingrowth is promoted. The highly porous metal used to form the graft 2 has a high strength-to-weight ratio and low stiffness and is capable of withstanding physiologic loading and minimizing stress. The porous metal may have, for example, a trabecular configuration. In one embodiment, the porous metal may include growth factors to further stimulate bone ingrowth. An example of a suitable graft is one formed from tantalum and vapour deposition techniquies. An example of a suitable commercially available porous metal includes but is not limited to, “TRABECULAR METAL,” available from Zimmer Technology, Warsaw, Ind.
In some embodiments, the tail 12 passes straight through the graft 2, in the longitudinal direction thereof. In other words, the length of the tail 12 is much greater than that of the graft 2, so that at least a substantial part of the tail 12 is anchored securely in the native layer of the glenoid surface G. As described in greater detail, in some embodiments the overall length of the tail 12 is adjustable to accommodate a variety of thicknesses of the graft 2 and/or geometry of the glenoid surface G.
In optional embodiments (not shown), the securing of the graft 2 to the glenoid surface G can be reinforced by fasteners additional to the tail 12, such as screws distributed around the tail 12 and passing through the graft 2 over at least part of the length thereof.
The humeral component 20 comprises a tail 21 for anchoring in the medullary cavity M of the humerus H. At its upper end, the tail 21 is provided with a head 22, also described as a humeral head, having, on its side opposing the tail 21, a concave articular face 22A in the form of a portion of a sphere, the radius of which is substantially equal to that of the face 11A. References to a humeral head should be interpreted to include a prepared or an unprepared natural humeral head as well as synthetic, or prosthetic humeral heads. When the prosthesis 1 is implanted, as shown in FIG. 1, the faces 11A and 22A are in mutual surface contact, thus allowing the various desired shoulder articular movements.
Given the presence of the graft 2, the face 11A is remote from the resected surface of the glenoid surface G in the sense that, if the graft 2 were omitted, the face 11A would be directly juxtaposed with the resected surface of the glenoid surface. Thus, on account of the graft 2, the glenoid articular face 11A and, accordingly, the humeral articular face 22A are laterally remote from the glenoid surface G, limiting the risk of the lower portion of the head 22 interfering with the bottom of the glenoid surface G, (e.g., with the pillar P of the scapula S). Thus, lateralization of the prosthesis 1 can be adjusted and modified based on the thickness of the graft 2. As the thickness of the graft 2 increases, the amount of lateralization also increases. In addition, it will be understood that, as a consequence resulting from this lateralization desired within the scope of the invention, the graft 2 acts as bone matter to make good any bone deficit in the glenoid surface.
In practice, the glenoid component 10 can be of a broad range of sizes, to which the graft 2 is adapted. Typically, the head 11 is available in at least two different sizes, namely with an external diameter of about 36 mm or about 42 mm, it being understood that other sizes are conceivable. Similarly, the length l of the graft 2 can have a broad range of values, distributed in practice in a uniform sequence, in a manner adapted to the morphology and/or to the pathology of the patient. The graft 2 can thus have lengths of about 3, 6, 8 or 10 mm, whereas the tail 12 has a length of between about 15 and about 25 mm, possibly greater.
A surgical method seeking to implant the shoulder prosthesis 1 of FIG. 1 will be described hereinafter, it being understood that the prosthesis in question is merely a non-limiting illustrative example of the method and the surgical instruments used to implant this prosthesis. In other words, the method and the instruments specified hereinafter can be used to implant shoulder prostheses of a broad range of structures, of which, for example, the glenoid and/or humeral components consist of a plurality of metallic, plastic and/or ceramic-type parts joined together. Thus it is possible, for example, to use a humeral component without an anchoring tail.
FIGS. 2-12 illustrate various methods and instruments for forming the graft 2 in situ. In a first stage of the operation, once the soft parts of the shoulder have been removed using a deltopectoral or supero-external approach, the shaft 31 of an ancillary instrument 30 is introduced into the medullary cavity M of the humerus H, passing straight through the upper epiphysis E of the humerus H, as illustrated in FIG. 2. In order to do this, the point of entry in the humeral epiphysis is determined beforehand by radiograph analysis of the face and profile of the humerus H.
In its common part, the shaft 31 is secured, in particular detachably, to a body 32 in the shape of an upwardly rounded bell. The body 32 is generally arranged transversely to the shaft 31, extending in length about a central geometrical axis 33. Projected in a plane mediolateral to the patient and containing the longitudinal axis of the shaft 31, as shown in FIG. 2, the central geometrical axis 33 is inclined relative to the longitudinal axis of the shaft at an angle α of between about 10 and about 70°, it being noted that, spatially, the two aforementioned axes do not necessarily intersect but cross in a somewhat mutually remote manner in an anteroposterior direction.
The body 32 has on its inside a concave surface 34, of which the main center of curvature and the peak pertain substantially to the central geometrical axis 33. The concave surface 34 is provided to reproduce approximately the surface features of the upper epiphysis of a normal anatomical humerus, it being understood that, in practice, the surgeon has a range of a plurality of homothetic ancillary instruments 30, the bodies 32 of which have respective dimensions associated with the size and the state of the patient's bones. On its outer face, the body 32 is provided with a protruding tube 35 centered on the central geometrical axis 33 and opening into the interior of the body 32, on its inner surface 34.
The shaft 31 is inserted into the medullary cavity M of the humerus H until contact is established between the inner surface 34 and the humeral epiphysis E, the body 32 then covering the epiphysis E in the manner of a cap. Then, advantageously, the shaft 31 is driven in rotation about itself, over a short course, in order to allow for the retroversion of the humerus H. In a manner known to those of skill in the art, the shaft 31 is provided, in its proximal end part, with diametral through-orifices 36 angularly offset from one another about the longitudinal axis of the shaft 31 and, as a function of the retroversion of the patient determined by the surgeon, an elongate rod (not shown) is introduced into one of these orifices in order effectively to display the retained direction of retroversion, so that the shaft 31 is rotated on itself until this retroversion rod is aligned with the patient's forearm.
A guide pin 40, at the pointed distal end 41, is then introduced into the tube 35, from the free end thereof, and is inserted into the humeral epiphysis E over a substantial depth, as indicated by arrow 42 in FIG. 2, until its point pierces and passes at least partially through the outer cortex of the humerus H. It will be understood that the ancillary instrument 30 allows the guide pin 40 to be inserted in a suitable direction relative to the humerus H, the tube 35 acting as a guide for introducing and feeding through the pin. In order to prevent interference between the guide pin 40 and the shaft 31, when the guide pin 40 passes through the central zone of the humerus H, the corresponding common part 37 of the shaft 31 advantageously tapers: the part 37 of the shaft 31 thus has a smaller cross-section than the proximal and distal end parts forming the remainder of the shaft 31.
Once the guide pin 40 has reached an insertion depth in, or even through, the humerus H sufficient securely to anchor it, the ancillary instrument 30 is withdrawn, without removing the guide pin 40. The humerus H is then in the state illustrated by solid lines in FIG. 3.
In a variation, when carrying out the first stage of the operation, the guide pin 40 is inserted in the humerus H without being guided, i.e. without using the ancillary instrument 30.
In a second stage, the surgeon will resect the end of the humeral epiphysis E using an ancillary instrument 50 illustrated in FIG. 3. This ancillary instrument 50 comprises a tubular body 51, the internal central bore in which has a diameter equal to the external diameter of the guide pin 40. At the distal end of the body 51, the ancillary instrument 50 comprises a planar cutter 52, extending in a plane substantially perpendicular to the longitudinal axis of the body 51. In the distal projection of the cutter 52 and in a manner centered on the longitudinal axis of the body 51, the ancillary instrument 50 further comprises a terminal drill 53 internally delimiting a central bore communicating with the bore in the body 51. The external diameter of the drill 53 is provided so as to be equal to the external diameter of the anchoring tail 12 of the glenoid component 10 to be implanted, for reasons which will become apparent hereinafter.
The surgeon threads the ancillary instrument 50 around the guide pin 40 by introducing it by the terminal drill 53 thereof, as indicated by arrow 54 in FIG. 3. When this drill reaches the end of the epiphysis E, it drills the bone matter so as to form a cylindrical recess E₁centered about the guide pin 40 and indicated by broken lines in FIG. 3. Similarly, as the ancillary instrument 50 moves downward along the guide pin 40, the cutter 52 gradually resects the end of the humeral epiphysis E, over a depth of a few millimeters, until there is obtained a cutting plane E₂perpendicular to the guide pin 40, also indicated by broken lines in FIG. 3.
In a third stage, once the ancillary instrument 50 has been removed from the guide pin 40, the surgeon will cut the humeral epiphysis E in a manner centered on the guide pin 40, i.e. he will shape the bone matter forming this epiphysis E into a cylinder E₃having a center axis E_X-Xcorresponding to the axis 33, as illustrated in FIG. 5. For this purpose, the surgeon uses an ancillary instrument 60 illustrated in FIG. 4. The ancillary instrument 60 comprises a central rod 61, bored internally in a manner complementary to the guide pin 40 and having an external diameter equal to that of the drill 53. The rod 61 carries, in its common part, a crown saw 62 which is of annular shape centered on the rod 61 and the distal end edge of which has teeth 63.
The rod 61 of the ancillary instrument 60 is slipped around the guide pin 40, which is left in place in the humeral epiphysis E, until its distal end is received in a complementary manner in the recess E₁. In doing this, the saw 62 gradually cuts out the bone matter from the epiphysis E so as to obtain the bone cylinder E₃, it being noted that a corresponding part of the recess E₁passes through the entire length of said bone cylinder. The length of the cylinder E₃thus obtained, i.e. its dimension along its axis E_X-X, is determined by the depth of action of the saw 62, wherein this depth can easily be marked along the rod 61, in particular by markings.
Once the ancillary instrument 60 has been removed, the humerus H is in the state illustrated in FIG. 5.
In a fourth stage, the surgeon will remove the cylinder of bone matter E₃from the humerus H using a cutting ancillary instrument 70 illustrated in FIGS. 6 and 7. This ancillary instrument 70 comprises a tubular block 71, the internal diameter of which is equal to that of the saw 62. At its distal end, the block 71 forms a protruding outer edge 72 in which there is delimited a transverse slot 73 opening into the internal volume of the block. At its proximal end, the block 71 is closed by a base wall 74, from the central zone of which there protrudes, inside the block, a centering stud 75, the external diameter of which is equal to that of the drill 53.
After having removed the guide pin 40, the ancillary instrument 70 is slipped around the humeral cylinder E₃, as indicated by arrow 76 in FIG. 7. The cylinder E₃is received in a complementary manner in the block 71 until the edge 72 rests against the bone surface surrounding the base of the cylinder E₃. A planar saw blade (not shown) is then introduced from outside into the slot 73 in order to cut the base of the cylinder E₃over a cutting plane E₄substantially perpendicular to the axis E_X-Xand indicated by broken lines in FIG. 7. During sawing, most of the cylinder E₃is protected by the block 71 and the base wall 74, it being noted that the stud 75 is accommodated in a complementary manner in the upper end part of the central recess E₁.
Once the ancillary instrument 70 has been removed, the surgeon recovers the cylinder of bone matter E₃thus separated from the humerus H.
In a non-illustrated variation, the slot 73 can be provided so as to be inclined relative to the longitudinal direction of the block 71 so that, in contrast to the cylinder E₃described hereinbefore, the bone cylinder thus obtained has longitudinal end faces inclined relative to one another. The graft 2 is thus able to make good the wear to a peripheral portion of the glenoid surface G, it being noted that the inclination of the slot 73 is advantageously adjustable as a function of the wear noted by the surgeon during the operation.
Before describing the following stage of the operation, namely the fifth stage, FIGS. 8 to 12, which illustrate a set of instruments forming a variation of the unit comprising the ancillary instrument 30, 50, 60 and 70 described hitherto, will now be considered.
Thus, FIG. 8 shows an ancillary instrument 130 as a variation of the ancillary instrument 30 from FIG. 2. The ancillary instrument 130 comprises a distal body 132 which is functionally similar to the body 32 of the ancillary instrument 30. In particular, the body 132 is designed to cover the upper humeral epiphysis E in the manner of a cap. Unlike the body 32 of the ancillary instrument 30, the body 132 is perforated, in particular to give the surgeon a better view of the humeral epiphysis when positioning the body 132. Like the body 32 of the ancillary instrument 30, the body 132 is provided with a proximal tube 135 projecting from its external face and centered on the axis 133 around which the body 132 extends.
The ancillary instrument 130 allows the guide pin 40 to be inserted in the humeral epiphysis E so as to be close-fitted relative to the humerus H, as indicated by the arrow 142 in FIG. 8.
As a variation of both the ancillary instrument 50 and the ancillary instrument 60 shown in FIGS. 3 and 4, an ancillary instrument 160 is shown in FIGS. 9 and 10. The ancillary instrument 160 comprises an elongate shaft 161 provided, at its distal end, with a crown saw 162 of annular shape centered on the shaft 161 and of which the distal end edge has teeth 163. The shaft 161 has an internal bore throughout its length so that it can be slipped, in a close-fitting and coaxial manner, around the guide pin 40 which is left in position in the humeral epiphysis E, as indicated by the arrow 164 in FIG. 9. Unlike the saw 62 of the ancillary instrument 60, the saw 162 has perforations in its lateral wall and comprises a base wall 165 which extends perpendicularly to the longitudinal direction of the shaft 161 and of which the distal face forms a planar reamer 166.
Hence, when the ancillary instrument 160 is slipped round the guide pin 40, the teeth 163 of the saw 162 gradually cut out the bone matter of the humeral epiphysis E so as to obtain the bone cylinder E₃. Once the entire height of the saw 162 has thus been introduced into the epiphysis, the reamer 166 begins to cut the upper end of this epiphysis and thus progressively resects this end until the cutting plane E₂is obtained.
Once the ancillary instrument 160 has been released, the humerus H is in the state shown in FIG. 11.
The surgeon then uses a drilling ancillary instrument 167 comprising a bored shaft 168 of which the distal end is provided with a drill 153. By slipping the shaft 168 around the guide pin 40, as indicated by the arrow 169 in FIG. 11, the surgeon, by the action of the drill 153, digs the central part of the cylinder of bone matter E₃round the guide pin 40 so as to form the recess E₁, centered on the axis E_x-xof the cylinder E₃, as indicated in broken lines in FIG. 12, in which the ancillary instrument 168 has been released.
In practice, the drilling ancillary instrument 167 can also be used after a variation of the ancillary instrument 50, depleted of the drill 53, has been used and/or after a variation of the ancillary instrument 60, of which the rod 61 does not project on the distal side of the base wall of the saw 62 has been used.
As a variation of the ancillary instrument 70 shown in FIGS. 6 and 7, FIG. 12 shows an ancillary instrument 170. The ancillary instrument 170 comprises an annular body 171 equipped at a point of its periphery with a proximal handling shaft 176. The annular body 171 is designed to be mounted on the humeral epiphysis E while surrounding the entire portion of the epiphysis in which the cylinder of bone matter E₃, previously cut out by the ancillary instrument 160, is delimited. On its distal side, the body 171 delimits a surface 173 for application and guidance of a bone cutting instrument, not shown, such as a saw blade or the like.
Hence, by manipulating the shaft 176, the surgeon positions the annular body 171 around the humeral epiphysis E so as to position the guide surface 173 in a suitable manner relative to the cylinder of bone matter E₃. The surgeon then applies the cutting instrument against this surface 173 in a guided manner in order to cut the base of the cylinder E₃over the cutting plane E₄and release this cylinder from the humerus H.
Advantageously, the guide surface 173 forms an angle of approximately 155 degrees with the longitudinal direction of the shaft 176, and this allows the ancillary instrument 170 also to be used to prepare the implantation of the humeral component 20 at a later stage, by positioning the shaft 176 in such a way that its longitudinal direction is substantially aligned with the longitudinal direction of the humerus H, as illustrated in FIG. 12.
In a fifth stage, the cylinder of bone matter E₃is used to form the graft 2 described hereinbefore. In order to do this, this cylinder is fitted on the glenoid surface G. The glenoid surface G is previously prepared for this purpose, being opened up and, if necessary, resected. The glenoid component 10 is then implanted in the configuration described hereinbefore with reference to FIG. 1. It will be understood that the anchoring tail 12 is introduced coaxially, in a substantially close-fitting manner, into the central recess E₁in the cylinder E₃.
If the longitudinal end faces of the bone cylinder have been formed so as to be inclined relative to each other, it will be understood that the interposing of this cylinder, as the graft, between the glenoid component 10 and the glenoid surface G allows inclination, in particular downward inclination, of the glenoid articular face 11A.
More generally, it will be understood that the dimensions desired by the surgeon for the graft 2, in particular as a function of the size of the glenoid component 10, determine the dimensions of the ancillary instruments 50, 60 and 70 or the ancillary instruments 160, 168 and 170 used to take the bone cylinder E₃from the humeral epiphysis E. In particular, the internal diameter of the saw 62 or 162 determines the external diameter of the graft 2. Similarly, the depth of action of this saw determines the length/of the graft while at the same time allowing for any adjustment in length resulting from the positioning of the sawing slot 73 or the guide surface 173.
Furthermore, the geometry desired for the longitudinal end faces 2B and 2C of the graft 2 directly conditions the embodiment of the resection ancillary instrument 50 and cutting ancillary instrument 70 or the ancillary instrument 160 and 170, in the sense that the parts of these ancillary instruments that determine the incision profile of the bone are shaped to form an appropriate incision in the humeral epiphysis. Optionally, these ancillary instruments 50 and 70 can be associated with one or more ancillary instrument for resurfacing the longitudinal end faces of the removed cylinder E₃.
In practice, the surgeon also takes account of the state of the cancellous bone matter forming the epiphysis E in order, if necessary, to remove the graft with as healthy a constitution as possible. For this purpose ancillary instrument for gripping and storing the graft 2 after it has been released from the humerus H can optionally be provided, in order to limit the risks of damaging the graft.
Furthermore, in non-illustrated variations, the graft 2 can have volume forms other than a cylinder as in the figures, provided that the volume of bone matter forming the graft 2 has a shape generally centered about a longitudinal axis of the type of the axis E_X-X, while at the same time defining a lateral face and longitudinal end faces of the type of the faces 2A, 2B and 2C. For example, the graft 2 can thus be truncated in shape, having a longitudinal axis E_X-X; in this case, the inner surface of the crown saw 62 or 162 is, for example, provided so as to be truncated.
Optionally, the graft 2 can be protected laterally by a reinforcing structure, such as for example ring 80 shown in FIG. 13. In practice, the ring 80 is configured to surround in an appropriate manner the lateral face 2A of the graft 2, over the entire length of this graft. The ring 80 is thus, in conjunction with the graft 2, interposed between the glenoid component 10 and the glenoid surface G. It will be understood that the ring 80 can, for example, be used if the graft 2 has, at least over a part of its length, an external diameter less than that of the glenoid head 11, the ring thus compensating for the difference in diameter.
If the ring 80 is implanted in conjunction with the graft 2, it protects the lateral face 2A of the graft 2 and forms a support for at least a part of the face 11B of the glenoid component 10, thus limiting the stresses applied to the graft 2. Advantageously, the ring 80 is covered with hydroxyapatite or, more generally, has a porous or honeycomb surface state allowing improved bone adhesion and rehabilitation of the ring 80 to the graft 2 and to the resected surface part of the glenoid surface G that is not covered by the graft 2. In one embodiment, the ring 80 is attached to the glenoid component 10.
In practice, it will be understood that the inner surface of the ring 80 is advantageously complementary with the face 2A of the graft 2, whereas its outer face can have advantageous optional configurations. The outer surface can thus be provided so as to be truncated and diverged toward the glenoid surface G, so holes passing through the ring 80 in respective directions substantially perpendicular to the outer surface thereof are able to receive screws or the like in order to reinforce the securing of the graft 2 to the glenoid surface G. Similarly, the bottom portion of the ring 80 can be provided so as to be less thick than the remainder of the ring so as not subsequently to disturb the humeral component 20 during adduction movements on the part of the patient.
In a variation of the fitting method, rather than delivering a one-piece bone volume such as the cylinder E₃, in the upper humeral epiphysis E, the graft 2 can consist of a purée of bone substance. This substance is taken from the spongy bone zones of the humeral epiphysis, in particular when preparing the humerus H for the fitting of the humeral implant. In practice, in order to contain this purée of bone substance during implantation of the glenoid component 10, a reinforcing structure, such as for example a lattice 90 shaped as a cage 92 for receiving this purée will advantageously be used, as shown in FIG. 14. The cage 92 is designed to be interposed between the glenoid component 10 and the previously prepared glenoid surface G, according to an arrangement similar to the one-piece graft illustrated in FIG. 1. In particular, the cage 92 has, for example, a generally cylindrical shape of which the external diameter corresponds to that of the glenoid head 11 and of which the length corresponds to the aforementioned length l.
The lattice 90 forming the cage 92 allows exchanges of biological fluids between the purée of bone substance with which the cage is filled and the surrounding tissues of the patient. The cage 92 thus prevents necrosis of the purée of bone substance while mechanically protecting it. In particular the cage 92 absorbs a proportion, or even the majority, of the stresses applied to the graft 2 consisting of the purée of bone substances by forming, in the region of its lateral end walls 92A and 92B, supports for the face 11B of the glenoid component 10 and the previously prepared surface of the glenoid surface G respectively. The bone substance preferably chemically bonds with the glenoid surface G through the lattice 90. In effect, the glenoid surface G is extended laterally outward to engage with the face 11B of the glenoid component 10.
In another embodiment, the cage 92 is constructed from a porous matrix or scaffold, without the purée of bone substance. The cage 92 can be, for example, reticulated bioceramic framework, structured porous tantalum, synthetic fiber mesh, and the like. The native bone of the glenoid surface G grows into the porous matrix or scaffold to create a graft with structure properties comparable to native bone. The cage 92 is alternately made of a slow-absorbing, biologically benign material, such as Poly-4-hydroxybutyrate (a.k.a. Tephaflex™), poly(urethane urea) (Artelon™), surgical silk, or other materials, known to the art, having similar characteristics, such as disclosed in U.S. Patent Publication No. 2007/0198087, entitled Method and Device for Rotator Cuff Repair, filed Feb. 5, 2007 and U.S. Patent Publication No. 2007/0276509, entitled Tissue Scaffold, filed Aug. 9, 2007, the entire disclosures of which are incorporated by reference. Other less preferred embodiments employ non-absorbable materials such as PTFE, Polypropylene, Nylon, or other biocompatible, inert materials known to the art.
Before or after implanting of the glenoid component 10, the humeral component 20 is implanted in the humerus H, advantageously using ancillary instrument (not shown), the handling of which is marked by the end part of the recess E₁remaining in the humeral epiphysis E after removal of the bone volume such as the cylinder E₃. If the surgical actions applied to the humerus H for implanting the component 20 by way of the recess E₁are dispensed with and these actions are therefore generally independent of those applied to the humerus for taking the graft 2, the ancillary instrument 30 can be simplified, as it is in this case no longer necessary to take account of the retroversion of the patient's forearm in order to insert the guide pin 40. The shaft 31 may in this case assume the form of an intramedullary humeral rod.
According to a variation of the fitting method, the graft 2, whether in the form of a one-piece bone volume or of a purée of bone substance, is not taken from the humeral epiphysis E but rather is taken from another of the patient's bones, in particular from his ilium, or consists of an allograft, a graft of synthetic origin or a graft of metallic origin, it being understood that the dimensions of this synthetic graft are provided so as to be appropriate for the glenoid component 10 to be implanted, as stated hereinbefore for the removed cylinder E₃or cone frustum. Obviously, the protection ring 80 and the cage 92 described hereinbefore can be used in conjunction with a graft of this type of alternative origin.
FIG. 15 is a schematic illustration of a glenoid component 200 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. The glenoid component 200 includes a recess 202 that substantially receives the graft 204. The recess 202 acts as a reinforcing structure that protects the graft 204 laterally, similar to the ring 80 in the embodiment of FIG. 13. Consequently, the graft 204 can be a one-piece bone volume, a purée of bone substance or formed from a synthetic or metallic material. In an embodiment where the graft 204 is a purée of bone substance, reinforcing fibers 279 are optionally added to the mixture. In the illustrated embodiment, lower portion 206 of the convex articular surface 208 extends beyond the pillar of the scapula S to minimize interference with the humeral prosthetic portion. The radius of curvature of convex articular surface 208 is preferably selected so the center of rotation 214 around the glenoid component 200 is preferably in plane 210 comprising a distal surface 212 of the graft 204 or between the plane 210 and the glenoid surface G. Once the graft 204 has fused with the glenoid surface G, the distal surface 212 of the graft 204 becomes the effective glenoid surface.
FIG. 16 is a schematic illustration of a glenoid component 220 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. A reinforcing structure 222 extends over at least a portion of the graft 224. The reinforcing structure 222 can be rigid or flexible. In one embodiment, the reinforcing structure 222 is constructed from a mesh material made from metal, synthetics, ceramics, or a combination thereof. Consequently, the graft 224 can be a one-piece bone volume, a purée of bone substance or formed from a synthetic or metallic material. Screws 226 optionally secure the reinforcing structure 222 and/or graft 224 to the glenoid surface G.
The glenoid component 220 includes a recess 230 that engages with distal surface 232 of the reinforcing structure 222. An anchor 234 optionally extends through the reinforcing structure 222 and graft 224 to further secure the glenoid component 220 to the scapula S. In the illustrated embodiment, the anchor 234 includes a pointed tip 236 to facilitate insertion into the glenoid surface G. The radius of curvature 228 of convex articular surface 235 is preferably selected such that the center of rotation 233 of the glenoid component 220 is preferably either in or behind plane 237 comprising a distal surface 239 of the graft 224. Once the graft 224 has fused with the glenoid surface G, the distal surface 239 of the graft 224 becomes the effective glenoid surface.
FIG. 17 is a schematic illustration of a glenoid component 240 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. A graft 242 is formed with a distal recess 244. An anchor 246 extends through the graft 242 into the glenoid surface G so that base plate 248 is positioned in the distal recess 244. A tension member 250 is optionally positioned in a center bore 252 of the anchor 246 to retain the base plate 248 against the glenoid surface G. A variety of glenoid components 240 can then be attached to the base plate 248 using a variety of attachment mechanisms. In one embodiment, the graft 242 is surrounded by reinforcing structure 257, such as for example a metal or synthetic mesh material. The radius of curvature of convex articular surface 258 is preferably selected so the center of rotation 259 around the glenoid component 240 is preferably in or behind a plane 254 comprising a distal surface 256 of the graft 242. Once the graft 242 has fused with the glenoid surface G, the distal surface 256 of the graft 242 becomes the effective glenoid surface.
FIG. 18 is a schematic illustration of a glenoid component 260 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. A graft 262 is secured to the glenoid surface G using base plate 264 and anchor 266. The glenoid component 260 includes a first recess 268 sized to engage with the base plate 264 and a second recess 270 so that extensions 272 of the convex articular surface 271 extend onto a portion of the scapula S. The extensions 272 can optionally be flexible or semi-flexible to facilitate implantation. In one embodiment, the extensions 272 are attached to the scapula S using adhesives, fasteners, and the like. The graft 262 can be a one-piece bone volume, a purée of bone substance or formed from a synthetic or metallic material. The radius of curvature of convex articular surface 271 is preferably selected such that the center of rotation 278 around the glenoid component 260 is preferably in or behind a plane 274 comprising a distal surface 276 of the bone graft 262.
FIG. 19 is a schematic illustration of a glenoid component 280 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. A bone graft 282 is located between the glenoid surface G and the opposing surface 284 of the glenoid component 280. In the illustrated embodiment, the bone graft 282 is two or more layers 282 a, 282 b of bone graft material. A tension member 286 is positioned in center bore 288 to retain the glenoid component 280 against the glenoid surface G. The radius of curvature of convex articular surface 290 is preferably selected so the center of rotation 296 is in or behind plane 292 comprising distal surface 294 of the bone graft 282.
FIG. 20 is a schematic illustration of a glenoid component 300 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. An adjustable anchor portion, also described as an anchor structure or tail portion, of the glenoid component 300 includes reinforcing structure 302, which is attached to the boney structure forming the glenoid surface G using fasteners 304. Side walls 303 of the reinforcing structure 302 support a bone graft 310 by engaging an outer lateral face 311 of the bone graft 310. The reinforcing structure 302 preferably has a plurality of holes or perforations 306 to facility bone in-growth.
The adjustable anchor portion also includes an opposite reinforcing structure 308 that extends over the reinforcing structure 302 and bone graft 310 and restricts lateral movement of the bone graft 310. Thus, the adjustable anchor portion is formed of two, opposing portions—the first and second reinforcing structures 304, 308. In the illustrated embodiment, the opposite reinforcing structure 308 telescopically engages with the reinforcing structure 302 to adjust an overall length of the reinforcing structure 308. The bone graft 310 has a distal face 312 and a medial face 313 and defines a thickness between the distal and medial faces 312, 313. The bone graft 310 can be a one-piece bone volume, a purée of bone substance, or any of the other materials previously described. The opposite reinforcing structure 308 optionally includes a plurality of holes 307 to facilitate bone in-growth.
In some embodiments, the glenoid component 300 includes an articulation surface 315A and an engagement surface 315B that is attached to distal surface 312 of the opposing reinforcing structure 308. In the illustrated embodiment, the glenoid component 300 is mounted to the opposing reinforcing structure 308 off-center. The opposing reinforcing structure 308 preferably has a plurality of mounting features that permit the surgeon to locate the glenoid component 300 in a variety of locations. The radius of curvature of convex articular surface 314 is preferably selected so the center of rotation 319 is in or behind plane 316 comprising distal surface 318 of the bone graft 310. In another embodiment, the center of rotation is close to the plane 316.
FIGS. 20A and 20B show additional glenoid components that include adjustable length tails, or anchoring structures for use with grafts having a variety of thicknesses, according to embodiments of the present invention. For example, in some embodiments, a surgeon or other user selects a desired bone graft thickness and adjusts the overall length of an anchoring portion of the glenoid component for use with that graft thickness. By adjusting the overall length of the anchoring structures, the glenoid components are better able to facilitate lateralization of the center of rotation of the glenoid component with a secure affixation into the boney structure forming the glenoid, for example, as well as additional or alternative advantages. In some embodiments, the bone graft is at least 7 mm thick, at least 10 mm thick, or from about 7 mm thick to about 10 mm thick, and the anchor portion is adjustable to at least 20 mm in length, at least 25 mm in length, or from about 20 mm in length to about 25 mm in length, although other dimensions are contemplated.
FIG. 20A shows a glenoid component 300A of an inverted shoulder prosthesis, according to an embodiment of the present invention. The glenoid component 300A includes a head 301A, also described as a head structure, which has a convex articular surface 302A of generally hemispherical shape and an opposing, engagement face 303A. The convex articular surface is adapted for engagement with a humeral head (e.g., a prosthetic humeral head or a natural humeral head that has been formed to define a complementary, concave humeral articular surface). In some embodiments, the opposing face 303A is generally planar although different configurations (e.g., concave or convex configurations) are contemplated. Although an inverted shoulder prosthesis configuration is shown, in other embodiments the glenoid component 300A is configured as a standard shoulder prosthesis with the articular surface 301A being substantially concave, for example.
As shown, the glenoid component 300A also includes an anchoring tail 304A, also described as an anchoring portion or anchoring structure, that extends transversely from the engagement face 303A and is adapted to be anchored in the glenoid surface G (FIG. 1) to secure the glenoid component to the scapula S (FIG. 1). In some embodiments, the anchoring tail 304A is provided with a base (not shown) adapted to be received inside the head 301A and secured thereto (e.g., via a press fit, complementary threads, adhesives, or other fastening means). In different terms, the connection between the tail 304A and the head 301A optionally includes material continuity (i.e., formation of a single piece of material, also described as a monolithic structure), respective wedging surfaces (e.g., a press fit), mechanical assembly structures (e.g., threading), and others.
As shown, the anchoring tail 304A defines an overall length and includes a first portion 305A having an inner lumen 306A, a second portion 307A, and a lock member 308A. The first portion 305A optionally has a substantially circular cross-section, although non-circular cross-sections (e.g., hexagonal or square), are contemplated. As described, the tail 304A is configured such that a user is able to telescope the second portion 307A in and out of the first portion 305A in order to adjust the overall length of the anchoring tail 304A. In some embodiments, the second portion 307A includes a conical threadform or a buttress threadform.
The inner lumen 306A of the first portion 305A optionally includes female threading (not shown). The second portion 307A is adapted to telescopically fit within the inner lumen 306A of the first portion 305A, the second portion 306A having male threading 309A according to some embodiments. The second portion 307A is optionally substantially cylindrical with a circular transverse cross-section, although other cross sections (e.g., hexagonal or square) are contemplated. The lock member 308A is optionally formed similar to a nut, with flats or other surface features. The overall length of the tail 304A is adjusted by rotating the second member within the first member to the desired overall length. The overall length is optionally locked by tightening the lock member 308 to help ensure the anchoring tail 304A remains at the desired length and does not back or forward rotate to a different overall length.
In some embodiments, a bone graft (not shown) such as those previously described, is received by the tail 304A, the bone graft optionally including a central aperture or other feature that fits over the tail that restricts lateral movement of the bone graft and secures the bone graft to the tail 304A, where the tail 304A receives the bone graft with a medial surface of the bone graft engaged with the engagement face 303A. In some embodiments, the bone graft is first received against the engagement face 303A and then the tail 304A is secured to the head 301A thereby securing the bone graft to the head 301A. In some embodiments, the bone graft is received over the first portion 305A of the tail 304A and then the second portion 306A is secured to the first portion 305A of the tail 304A.
FIG. 20B shows a glenoid component 300B of an inverted shoulder prosthesis, according to some other embodiments. The glenoid component 300B includes a head 301B which has a convex articular surface 302B of generally hemispherical shape and an opposing face 303B. In some embodiments, the opposing face 303B is generally planar although different configurations (e.g., concave or convex configurations) are contemplated. Although an inverted shoulder prosthesis configuration is shown, in other embodiments the glenoid component 300B is configured as a standard shoulder prosthesis with the articular surface 302B being substantially concave, for example.
As shown, the glenoid component 300B also includes an anchoring tail 304B that extends transversely from the face 302B and is adapted to be anchored in the glenoid surface G (FIG. 1) to secure the glenoid component to the scapula S (FIG. 1). In some embodiments, the anchoring tail 304B is provided with a base (not shown) adapted to be received inside the head 301B and secured thereto (e.g., via a press fit, complementary threads, adhesives, or other fastening means). In different terms, the connection between the tail 304B and the head 301B optionally includes material continuity (i.e., formation of a single piece of material, also described as a monolithic structure), respective wedging surfaces (e.g., a press fit), mechanical assembly structures (e.g., threading), and others.
As shown, the anchoring tail 304B defines an overall length and includes a first portion 305B having an inner lumen 306B and a second portion 307B. The second portion 307B is optionally interchanged with a similar component having a substantially different configuration, such as a different length. For example, a third portion 308B is shown which may be substituted for the second portion 307B. Additional components, of different lengths, widths, cross-sections, or other alternate configurations that are adapted to be secured to the first portion 305B are also available according to some embodiments.
The first portion 305B optionally has a substantially circular cross-section, although non-circular cross-sections (e.g., hexagonal or square), are contemplated. As alluded to in the foregoing description, the tail 304B is configured such that a user is able to select between a plurality of extensions (e.g., between second and third portions 307B, 308B) in order to adjust the overall length of the anchoring tail 304B. The inner lumen 306B of the first portion 305B optionally includes female threading (not shown). In some other embodiments, the first portion 305B includes male threading for mating with female threading on the second portion 307B and/or third portion 307C.
In some embodiments, the second portion 307B has a narrowed region 309B with male threading adapted to form a complementary fit with the female threading of the first portion 305B. The second portion 307B is optionally substantially cylindrical with a circular transverse cross-section, although other cross sections (e.g., hexagonal or square) are contemplated. As shown, the second portion 307B has a length that is substantially longer than that of the third portion 308B. Thus, a user desiring to adjust the overall length of the anchoring tail 304B is able to not attach any additional component to the first portion 305B (i.e., utilize the non-extended length of the anchoring tail 304B), or select between securing one of a plurality of additional components of different lengths (e.g., the second and third portions 307B, 308B) to the first portion 305B to extend the overall length of the anchoring tail 304B.
In some embodiments, a bone graft 309B such as those previously described, is received by the tail 304B, the bone graft optionally including a central aperture or other feature that fits over the tail that restricts lateral movement of the bone graft and secures the bone graft to the tail 304B. As shown in FIG. 20B, the bone graft 309B has a central aperture 310B and defines a medial face 311B, a distal face 312B, and a thickness between the medial and distal faces 311B, 312B. As shown, the tail 304B receives the bone graft 309B with the medial surface 311B engaged with the engagement face 303B. As shown, the aperture 310B and the tail 304B have substantially complementary transverse cross-sections, although other configurations are contemplated.
In some embodiments, the bone graft 309B is first received against the engagement face 303B and then the tail 304B is secured to the head 301B thereby securing the bone graft to the head 301B. In some embodiments, the bone graft 309B is received over the first portion 305B of the tail 304B and then the second portion 306B is secured to the first portion 305B of the tail 304B.
FIG. 21 is a schematic illustration of a glenoid component 320 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. The glenoid surface G is resected at an angle 322 with respect to the medial line M of the patient. In order to compensate, the bone graft 324 is formed with non-parallel faces 326, 328. In the illustrated embodiment, the bone graft 324 is secured to the glenoid surface G using fasteners 330, although any of the structures disclosed herein could be used. The radius of curvature of convex articular surface 332 is preferably selected so the center of rotation 338 is in or behind plane 334 comprising distal surface 336 of the bone graft 324.
FIG. 22 is a schematic illustration of a glenoid component 340 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. The exposed surface 342 of the glenoid surface G is non-planar. In order to compensate, the bone graft 344 is preferably formed with a complementary shaped surface 346. In the illustrated embodiment, opposing face 348 of the glenoid component 340 also is non-planar. Consequently, distal surface 350 of the bone graft 344 is also preferably formed with a complementary shape. The non-planar surfaces 346, 348 provide structural advantages for some applications.
In the illustrated embodiment, the glenoid component 340 is secured to glenoid surface G using a plurality of fasteners 352. Although distal surface 354 of the glenoid component 340 is illustrated as planar it can be configured for with either a convex or concave articular surface, depending on the application.
FIG. 23 is a schematic illustration of a glenoid component 360 of an anatomical shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. An opposing face 362 of the glenoid component 360 is non-planar. In order to compensate, distal surface 364 of the bone graft 366 is preferably formed with a complementary shape. In the illustrated embodiment, the glenoid component 360 is secured to glenoid surface G using anchor 368, although any of the securing structures disclosed herein may be used. A distal surface 370 of the glenoid component 360 is illustrated as concave, but could be convex depending on the application.
FIG. 24 is a schematic illustration of a glenoid component 380 of an anatomical shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. An opposing face 382 of the glenoid component 380 is non-planar and keel 384. The keel 384 optionally includes holes 390 to facilitate bone in-growth. A distal surface 386 of the bone graft 388 is preferably formed with a shape complementary to opposing surface 382. The bone graft 388 can be a one-piece bone volume or a purée of bone substance. In one embodiment, a cut-out is formed in the bone graft 388 to receive the keel 384. In another embodiment, the bone graft 388 is an annular ring and the keel is located in the center opening and secured using a purée of bone substance, bone cement, or a variety of adhesives.
FIG. 25 is a schematic illustration of a glenoid component 400 of an anatomical shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. An exposed surface 402 of the glenoid surface G is non-planar. In the illustrated embodiment, the exposed surface 402 has a shape complementary to keel 404 on opposing face 406 of the glenoid component 400.
FIG. 26 is a schematic illustration of a glenoid component 420 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. An exposed surface 422 of the glenoid surface G is non-planar. In one embodiment, the various shapes 424 a, 424 b, 424 c, 424 d (collectively “424”) illustrated in FIG. 26 are formed in the glenoid surface G, such as for example to remove defects in the surface of the glenoid surface G and to increase the stability of the glenoid component 420.
The bone graft 426 can be a one-piece volume, a plurality of pieces, purée of bone substance, or a combination thereof. In one embodiment, a plurality of pre-formed bone grafts of known shape are available to the surgeon during the procedure. The surgeon removes material from the exposed surface 422 of the glenoid surface G corresponding to the shape of one of the pre-formed bone grafts. The surgeon then places the pre-formed bone graft into the corresponding recess formed in the glenoid surface G.
FIG. 27 is a schematic illustration of a glenoid component 440 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. The glenoid component 440 includes a recess 442 that engaged with base plate 444. The bone graft 458 can be a one-piece bone volume or a purée of bone substance.
In the illustrated embodiment, anchor 446 of the base plate 444 and/or the glenoid component 440 are located off-set from the center axis 448 of the glenoid surface G. Lower portion 450 of the convex articular surface 452 extends beyond the pillar of the scapula S to minimize interference with the humeral prosthetic portion. The radius of curvature of convex articular surface 452 is preferably selected so the center of rotation around the glenoid component 440 is preferably in a plane 454 comprising a distal surface 456 of the bone graft 458 or between the plane 454 and the glenoid surface G.
In the illustrated embodiment, the exposed surface 460 of the glenoid surface G includes one or more defects 462. These defects 462 are preferably repaired with a one-piece bone graft, a plurality of pieces, purée of bone substance, or a combination thereof 464. After the repair, the exposed surface 460 of the glenoid surface G is preferably generally planar and well suited to receive the bone graft 458.
FIG. 28 is a schematic illustration of a glenoid component 480 of an inverted shoulder prosthesis attached to the glenoid surface G according to an embodiment of the present invention. End faces 482, 484 of the bone graft 486 are not parallel. In the illustrated embodiment, an anchor 488 of the glenoid component 480 is at an angle with respect to horizontal axis 490 of the glenoid surface G. As a result, a surface 492 of the bone graft 486 acts as an extension of a lower portion of the convex articular surface 494.
FIG. 29 is a schematic illustration of the glenoid component 480 of FIG. 28 with the anchor 488 at a different angle with respect to the horizontal axis 490 of the glenoid surface G. Surface 496 of the bone graft 486 acts as an extension of an upper portion of the convex articular surface 494.
FIGS. 30A-30F illustrate an alternate method and apparatus for forming a bone graft 500 ex vivo in accordance with an embodiment of the present invention. The humeral epiphysis E is resected from the humerus H (see e.g., FIG. 7). In the illustrated embodiment, the resected humeral epiphysis E includes a planar surface P created during the resection and a curvilinear surface C.
The curvilinear surface C of the humeral epiphysis E is located on base 502, as illustrated in FIG. 30A. A cover 504 illustrated in FIG. 30B secures the humeral epiphysis E to the base 502. As illustrated in FIG. 30C, boring instrument 506 is inserted through opening 508 in the cover 504. The boring instrument 506 may be operated by hand or a motorized driver. In an alternate embodiment, the instrument 506 is an impaction instrument that does not include teeth 510.
In one embodiment, the resulting bone graft 500 is an annular ring with a planar surface 512 and a curvilinear surface 514 as illustrated in FIG. 30D. In an alternate embodiment, cutting instrument 516 is inserted through slot 518 in cover 504 so that the bone graft 500 is an annular ring with opposing planar surfaces, as illustrated in FIG. 30F.
Various modifications and additions can be made to the exemplary embodiments discussed without departing from the scope of the present invention. For example, the distal surfaces of the glenoid components disclosed herein can be used with an interpositional implant, such as disclosed in U.S. Pat. Nos. 6,436,146; 5,723,018; 4,846,840; 4,206,517; and U.S. Provisional Application Ser. No. 61/015,042, entitled INTRA-ARTICULAR JOINT REPLACEMENT, the complete disclosures of which are hereby incorporated by reference. While the embodiments described above refer to particular features, the scope of this invention also includes embodiments having different combinations of features and embodiments that do not include all of the described features. Accordingly, the scope of the present invention is intended to embrace all such alternatives, modifications, and variations as fall within the scope of the claims, together with all equivalents thereof.

Claims

1. A shoulder prosthesis adapted for implantation in a glenoid of a patient, the prosthesis comprising:

a head portion having an articulation surface adapted for articulation with a humeral head and an engagement surface opposite the articulation surface;

a bone graft having a medial surface and a distal surface and defining a thickness between the medial and distal surfaces, the medial surface having a shape complementary to the glenoid surface and the distal surface having a shape complementary to the engagement face of the head portion; and

an anchor structure connected to the engagement surface and adapted to extend through the bone graft and into the glenoid surface, the anchor structure being adjustable in overall length to accommodate the thickness of the bone graft such that the anchor structure extends through and projects beyond the bone graft upon engagement of the distal surface of the bone graft with the engagement surface of the head portion.

2. The prosthesis of claim 1, wherein the bone graft is at least 7 mm thick.

3. The prosthesis of claim 1, wherein the anchor structure is adjustable to at least 20 mm in length.

4. The prosthesis of claim 1, wherein the anchor structure includes a first portion and a second portion telescopically received in the first portion, the second portion being extendable from the first portion to adjust the overall length of the anchor structure.

5. The prosthesis of claim 1, wherein the anchor structure includes a first portion having a first length and a second portion releasably connected to the first portion to extend the overall length of the anchor structure.

6. The prosthesis of claim 1, wherein the bone graft includes metal material having a trabecular structure.

7. The prosthesis of claim 1, wherein the bone graft includes structured porous tantalum.

8. The prosthesis of claim 1, wherein the bone graft is taken from a bone in the patient.

9. The prosthesis of claim 1, wherein the bone graft comprises an upper epiphysis of a humerus.

10. The prosthesis of claim 1, wherein the bone graft comprises at least one of an allograft, a xenograft, a natural material, and a synthetic material.

11. The prosthesis of claim 1, wherein the bone graft defines an outer lateral face and the prosthesis further comprises a reinforcing structure that at least partially surrounds the outer lateral face of the bone graft.

12. The prosthesis of claim 1, wherein the bone graft defines an outer lateral face and the glenoid component at least partially surrounds the outer lateral face of the bone graft.

13. The prosthesis of claim 1, wherein the bone graft defines an outer lateral face and the prosthesis further comprises a reinforcing structure located between the medial surface of the bone graft and the glenoid surface, the first reinforcing structure comprising first side walls supporting the outer lateral face of the bone graft.

14. A shoulder prosthesis system adapted for replacement of a glenohumeral joint of a patient, the prosthesis comprising:

a humeral head having a humeral articulation surface; and

a glenoid component including:

a head portion having an articulation surface in articulating engagement with the humeral articulation surface of the humeral head;

a bone graft having a medial surface and a distal surface and defining a thickness between the medial and distal surfaces; and

an anchor structure connected to the engagement surface and secured into a glenoid surface of the glenohumeral joint, the anchor structure engaging the bone graft and restricting lateral movement of the bone graft, the anchor structure being adapted to be adjusted in overall length to accommodate the thickness of the bone graft.

15. The system of claim 14, wherein the anchor structure includes a first portion and a second portion, the second portion being telescopically received in the first portion and extendable from the first portion to adjust the overall length of the anchor structure.

16. The system of claim 14, wherein the anchor structure includes a first portion and a second portion releasably secured to the first portion to extend the overall length of the anchor structure.

17. A method of repairing a glenohumeral joint, the method comprising:

receiving a bone graft with an anchor structure of a glenoid component, the bone graft having a thickness between a medial surface and a distal surface of the bone graft;

engaging the medial surface of the bone graft with an engagement surface of a head structure of the glenoid component, the head structure having an articulation surface that is adapted to articulate with a humeral head, the articulation surface being positioned opposite the engagement surface;

restricting lateral movement of the bone graft with the anchor structure of the glenoid component, the anchor structure of the glenoid component projecting from the engagement surface of the glenoid component;

adjusting an overall length of the anchor structure of the glenoid component to compensate for the thickness of the bone graft; and

securing the anchor structure of the glenoid component into a boney structure of the glenoid.

18. The method of claim 17, further comprising engaging the articulation surface of the glenoid component with a natural humeral head.

19. The method of claim 17, further comprising engaging the articulation surface of the glenoid component with a prosthetic humeral head.

20. The method of claim 17, further comprising shaping a natural humeral head to define a humeral engagement surface and engaging the articulation surface of the glenoid component with the humeral engagement surface.

21. The method of claim 17, wherein the anchor structure includes a first portion having a first length and a second portion releasably connected to the first portion to extend the overall length of the anchor structure, and further wherein the bone graft is received by the first portion and then the second portion is releasably connected to the first portion.

22. The method of claim 17, wherein the bone graft is received by the engagement surface and then the first portion of the anchor structure is connected to the head structure.