This application claims priority under 35 U.S.C. §§119(a)-(d) to French Patent Application No. 08 58093 filed on Nov. 28, 2008, the entire contents of which are incorporated herein by reference.
Embodiments of the present invention relate to an instrument for fitting compression staples, to an assembly for fitting a compression staple, and to a method of fitting a compression staple to compress, fuse, join, span, and/or unite two bone portions.
A compression staple is used to hold two bone portions in a relative position in order to reinforce them and hold them in position. Such a compression staple conventionally comprises two branches interconnected by a transverse bridge, the branches being designed to be inserted in the bone portions on either side of the site of a fracture or an osteotomy in a bone that is to be repaired. The two branches of such a staple are designed to be moved towards each other so as to enable them to press the two bone portions against each other with a certain amount of pressure.
EP-A-1 870 042 describes a device for fitting compression staples that are made of a shape memory material, with branches that converge in the rest configuration of the staple. That device comprises a spreader part of trapezoidal shape for spreading the initially converging branches of the staple into a configuration for implanting the staple in a bone. The spreader part is positionable, while a staple is being fitted, between the branches of the staple on the side of the bridge that faces towards the branches. While the staple is being fitted, it is initially impacted partially into the bone portions, while the branches are held apart by the spreader part. The spreader part is then separated from the staple. Finally, the staple is impacted fully into the bone portions. Such a device thus requires two successive steps of impacting the staple, thereby lengthening the time taken to implant it. Furthermore, a staple made of shape memory material does not permit control of the compression load that is applied to the bone portions when the staple is in its implanted configuration.
Embodiments of the present invention include an instrument and an assembly for fitting compression staples that permit a compression staple to be implanted easily in bone portions for consolidation (e.g. compression and/or fusing), with the time required for implanting the staple being limited and with it being possible to control the amount of compression that is applied to the bone portions.
To this end, embodiments of the invention include an instrument for fitting compression staples, the instrument comprising a distal receiver portion for receiving a compression staple that comprises two branches interconnected by a transverse bridge, the instrument being characterized in that it further comprises:
According to embodiments of the present invention, the staple may be deformed by applying stresses solely to the bridge of the staple, and more precisely via three bearing regions that are distributed along the bridge, e.g. one of its end portions, its central portion, and its opposite end portion. The stresses are applied in opposing manner firstly to the central portion and secondly to the two end portions, so as to cause the staple to deform plastically in controlled manner in order to apply compression to the two bone portions interconnected by the staple. The surgeon can thus control the magnitude of the plastic deformation, it being understood that the compression staple used is made for example of stainless steel or of titanium, which is not possible with staples made of shape memory material, where the magnitude of the compression load is pre-imposed. In addition, by acting solely on the bridge of the staple, the staple can be put into place in a single operation, e.g. by acting on the bridge while the branches of the staple are already fully engaged in the bone, unlike existing equipment that requires the staple to be pushed in with two successive procedures. Positioning the staple in a single movement also makes it possible to control the extent to which the free ends of the branches of the staple project from the cortical bone opposite from that against which the bridge is placed: in order to achieve bone compression under good conditions, it is preferable for the branches of the staple to pass right through the two bone portions that are to be consolidated, and for this to occur before beginning to apply compression, whereas at the end of fitting, it is desirable for the free ends of the branches to project as little as possible from the cortex of said bone portions in order to limit injury to soft tissue, according to embodiments of the present invention.
In practice, embodiments of the invention can operate in two different ways depending on whether the zone of the bridge that is held stationary is its central portion or its two end portions, with deformation stress being applied to the other one of the two zones, the respective specifications for these two embodiments being presented in greater detail below with the help of two examples.
In one embodiment, when the first and second zones of the bridge of the staple correspond respectively to the end portions and to the central portion of the bridge, the deformation tool and the holder are adapted to apply their forces respectively on the two side faces of the bridge. Under such circumstances, deforming stress is applied to the central portion by acting in opposing manner on the sides of the bridge so that the bridge tends to bend in its central portion while remaining overall in a plane that is perpendicular to its branches, thereby causing the branches of the staple to move towards each other, and thus applying compression between the two bone portions in which the branches are inserted.
Such an embodiment may include one or more of the following characteristics, taken in isolation or in any technically feasible combination:
In another embodiment, when the first and second zones of the bridge of the staple correspond respectively to the central portion and to the end portions of the bridge, the deformation tool is adapted to apply its forces on the front face of the bridge that is remote from the branches, the holder preferably being adapted to co-operate with the central portion of the bridge solely on the side of the bridge that faces away from the branches. Under such circumstances, deformation stress is applied to the two end portions by acting in deformation on the front side of the bridge facing away from the branches, such that under the effect of a driving force applied to the end portions, the distal ends of the branches move towards each other, thereby generating a force urging the bone portions in which the branches are inserted towards each other and/or compressing them together.
Such an embodiment may include one or more of the following characteristics, taken in isolation or in any technically feasible combination:
An assembly for fitting a compression staple according to embodiments of the present invention includes the compression staple having two branches interconnected by a transverse bridge, and also an instrument as described above.
A method of fitting a compression staple to compress, fuse, join, span, and/or unite two bone portions according to embodiments of the present invention includes:
While multiple embodiments are disclosed, still other embodiments of the present invention will become apparent to those skilled in the art from the following detailed description, which shows and describes illustrative embodiments of the invention. Accordingly, the drawings and detailed description are to be regarded as illustrative in nature and not restrictive.
The characteristics and advantages of the invention appear in the following description of two embodiments of an instrument and an assembly of the invention for fitting a compression staple, given purely by way of example and with reference to the drawings, in which:
While the invention is amenable to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and are described in detail below. The intention, however, is not to limit the invention to the particular embodiments described. On the contrary, the invention is intended to cover all modifications, equivalents, and alternatives falling within the scope of the invention and of the appended claims.
The staple 6 is constituted by two elongate branches 7 and by a transverse bridge 8 interconnecting the proximal ends 72 (
Prior to being implanted in a bone, the staple 6 is in an initial configuration as shown in
According to embodiments of the present invention, for the reasons set out below, the staple 6 does not present any sharp edge, in particular along its branches 7. In one embodiment, the cross-section of each branch is not exactly square, in the sense that the four corners of the sections are significantly rounded, typically presenting a radius of curvature of 0.3 millimeters. In practice, to make the edges of the staple less sharp, at the end of fabrication, the staple is subjected to polishing, and in particular to a tumbling method that consists in tumbling the staples together with abrasive particles in a drum.
As shown in
The branch 3 is constituted by a proximal portion 31 enabling the instrument 2 to be held, an intermediate portion 32 mechanically connected to the branch 4 by a hinge pin on the axis Z2, and a distal portion 33 adapted to receive the staple 6, as explained in detail below. According to such embodiment, the portions 32 and 33 of the branch 3 extend generally rectilinearly one in line with the other along a proximal-distal axis X3 in
As illustrated in
Between the two housings 35, the distal end 34 of the portion 33 of the branch 3 is recessed, as shown in
The branch 4 of the instrument 2 is likewise constituted by a proximal portion 41 for holding the instrument 2, an intermediate portion 42 assembled to the portion 32 of the branch 3 in a hinged manner, and a distal portion 43 adapted to apply deforming forces to the staple 6. For this purpose, the side of the distal end 44 of said portion 43 that faces towards the distal portion 33 of the branch 3 is given a rounded shape presenting a convex surface 44A. In the example under consideration, and in section across the branch 4, this convex surface 44A presents a V-shaped profile with a rounded tip as illustrated in
As illustrated in
Initially, a bore 91 is drilled in each of the two bone portions 9 on either side of the site F of the fracture or the osteotomy of the bone. When the bone portions face each other without compression, as shown in
Advantageously, and for reasons that are explained below, the bores 91 are not drilled in the anatomically upper faces of the bone portions 9, but in one of the anatomical side faces of the bone, in particular its side face that is easier for the surgeon to reach.
Before, simultaneously with, or after drilling the bores 91, the staple 6 in the initial configuration for implantation is positioned on the distal end 33 of the branch 3. For this purpose, the distal ends 33 and 43 of the branches 3 and 4 are moved apart from each other, by moving their proximal portions 31 and 41 apart by pivoting about the axis Z2. The bridge 8 of the staple is then put into place in such a manner that its end portions 85 are received in respective ones of the housings 35, with the side face 87 and the front face 86 of the bridge bearing respectively against the surfaces 35B and against the surfaces 35A of these housings 35 at the bridge portions 85. As can be seen in
In order to hold the staple 6 stationary relative to the branch 3, the distal portions 33 and 43 of the branches 3 and 4 are moved progressively towards each other, by moving their proximal portions 31 and 41 in corresponding manner by pivoting about the axis Z2, until the distal end 44 of the portion 43 comes into contact against the side face 88 of the bridge 8 in the central portion 83 thereof, but without stressing there against. The instrument 2 is then in the configuration of
Once the staple 6 is held in this way relative to the instrument 2, the branches 7 are inserted into the bores 91. To do this, the distal end 71 of each branch is positioned facing a respective one of the bores 91, and then a thrust force is exerted via the branch 3 against the end portions 85 of the bridge 8 via the surfaces 35A of the housings 35. Each branch 7 then penetrates into the corresponding bore 91 until the front face 82 of the bridge 8 that faces towards the branches 7 comes into contact against the anatomical side surfaces of the bone portions 9, as shown in
Once the branches 7 have been inserted (e.g. maximally) into the bores 91, the staple 6 is deformed so as to put the bone portions 9 into compression. For this purpose, the instrument 2 is actuated so as to bring the proximal portions 31 and 41 of the branches 3 and 4 closer together. By tilting about the axis Z2 of the hinge pin, as represented by arrow G in
Insofar as the travel direction H (
It will be understood that the bending of the central portion 83 causes the end portions 85 to move towards each other, and thus causes the branches 7 to move towards each other. In other words, the distance between the axes decreases, thereby generating forces J causing the bone portions 9 to approach each other, as shown in
In practice, the relative movement of the end portions 85 of the bridge 8 towards each other is guided by the bottom surfaces 35B of the housings 35, thus enabling the branches 7 to be kept parallel in the mean plane π of the staple 6. Since the branches 7 are kept parallel to each other in the configuration for putting the staple 6 into compression, these two branches contribute over their entire length to the compression forces J, according to embodiments of the present invention. The facing ends 35C of the surfaces 35B of the two housings 35 may be shaped to allow the branches 7 to turn freely about their respective axes X7, as represented by arrows K in
After the staple 6 has been deformed in this way, the branch 4 is moved away from the branch 3 and then the instrument 2 is removed. Beforehand, if necessary, a small amount of impacting may be performed on the bridge 8 of the staple 6 in order to fully absorb any residual clearance between the face 82 of the bridge and the side faces of the bone portions 9 that might appear while bending the central portion 83.
In this way, the instrument 2 enables compression to be applied to the bone portions 9 while the staple 6 is already maximally engaged in the bone, e.g. when the bridge 8 of the staple is in contact with the surface of the bone. The retention by the distal portion 33 of the branch 3, and the deformation by the initial portion 43 of the branch 4 are not obtained by acting on the side of the bridge that faces towards the branches 7, but solely by acting on the side faces 87 and 88 in the end portions 85 and the central portion 83 of the bridge, according to embodiments of the present invention. Furthermore, the instrument 2 permits the compression force applied to the bone portions 9 by the staple 6 to be controlled, since the magnitude of the thrust force P is directly under the control of the surgeon acting on the branches 3 and 4. Thus, after applying a first magnitude of deformation on the staple, the surgeon can apply a greater magnitude to deform the staple more, e.g. to cause its central portion 83 to bend more and thus to reinforce the compression forces J, should that be necessary. At the most, the central portion 83 can thus be bent until the side face 88 of the bridge 8 is pressed in complementary manner against the surface 37A of the housing 37. Furthermore, regardless of how strongly the surgeon moves the proximal portions 31 and 41 of the branches 3 and 4 towards each other, this ensures that there is no risk of the surgeon breaking the bridge 8, according to embodiments of the present invention.
It should be observed that the space occupied by the bridge 8, in particular when its central portion 83 is bent, is particularly small, according to embodiments of the present invention. The risk of discomfort under the skin is therefore limited, as is the risk of tissue close to the staple 6 being injured. Furthermore, depending on which side face 87 or 88 of the bridge 8 the surgeon decides to apply the thrust force P, the central portion 83 is bent exclusively to one side or to the other side of the mean plane π of the staple 6. Thus, in the embodiment shown in
The instrument 2 and the associated staple 6 may include one or more alterations and/or variations, according to embodiments of the present invention. For example:
The staple-fitter assembly 101 shown in
The staple 106 has two branches 107 of elongate shape and a transverse bridge 108 interconnecting the two branches. In this embodiment, the staple is made of stainless steel. In a variant, the staple could be made of any other suitable material, e.g. out of titanium.
Prior to being implanted in a bone, the staple 106 is in an initial implantation configuration, as shown in
Because of the mechanical properties of the material from which it is made, the staple 106 is suitable for being deformed from its initial implantation configuration to a compression-applying configuration, as shown in
The staple 106 is deformed from its initial implantation configuration to its compression-applying configuration by applying a thrust force P on each end portion 185 of the bridge 108 that is connected to a branch 107, as shown in
The instrument 102 for fitting the staple 106 in the bone portions comprises a main body 103 of elongate shape having a longitudinal axis referenced X103. The main body 103 has a distal rod 131 and a tubular element 137 engaged around a proximal end portion 135 of the rod 131. As shown in
The staple 106 is designed to be positioned on the staple receiver portion 133 with the bridge 108 received bearing against a side face 133A of the receiver portion 133 and with the branches 107 projecting distally from the receiver portion 133, as can be seen in particular in
The instrument 102 also has a part 104 for deforming the staple 106 from its initial implantation configuration towards its compression-applying configuration. The deformation part 104 is movable in translation relative to the rod 131 parallel to the longitudinal axis X103 between a first position, visible in
The deformation part 104 has a cylindrical proximal portion 145 that guides the deformation part 104 in movement in translation relative to the rod 131 along the axis X103. The deformation part 104 also has a distal cap 141 arranged solely facing the face 133A of the receiver portion 133. As illustrated in
The profile of the cap 141 is designed in such a manner that when the deformation part 104 is in an intermediate position between its first and second positions, as can be seen in
A compression spring 110 is located between a shoulder 131A of the rod 131 and an internal radial shoulder 147 of the proximal portion 145 of the deformation part 104. The spring 110 urges the deformation part 104 elastically towards its first position, in which the cap 141 is offset on the proximal side parallel to the axis X103 relative to the face 133A of the receiver portion 133.
To actuate movement in translation of the deformation part 104 from its first position towards its second position, against the spring 110, the instrument 102 includes a lever 105 pivotally mounted on the distal portion 135 of the rod 131 about an axis X105 perpendicular to the translation axis X103. The lever 105 defines an eccentric cam 151 for co-operating with the proximal end 149 of the deformation part 104. The lever 105 is suitable for being moved from an initial position in which a small-diameter cam surface 152 of the eccentric cam 151 co-operates with the proximal end 149 of the deformation part 4, thereby forming an abutment for holding the deformation part 104 in its first position, and a maximally actuated position in which a cam surface 145 of the eccentric cam 151 having a diameter greater than the diameter of the cam surface 152 cooperates with the proximal end 149 of the deformation part 104 and holds the deformation part 104 in its second position. The diameter of the peripheral surface of the eccentric cam 151 increases continuously between its surfaces 152 and 154, according to embodiments of the present invention.
A method according to embodiments of the present invention includes fitting the compression staple 106 of the staple-fitter assembly 101 with the instrument 102 for the purpose of joining and compressing two bone portions 9 of a bone that has fractured or that has been subjected to an osteotomy, e.g. a phalanx or a metatarsus.
Firstly, a bore 91 is drilled in each of the two bone portions 9 on either side of the site F of the bone fracture or osteotomy. Advantageously, in the configuration in which the bone portions 9 touch each other without compression, as shown diagrammatically in
Before, simultaneously with, or after drilling the bores 91, the staple 106 in its initial implantation configuration is positioned on the receiver portion 133 of the instrument 102. For this purpose, where necessary, the instrument 102 is set into its configuration that is shown in
The central portion 183 of the bridge 108 of the staple is then held stationary relative to the receiver portion 133 by actuating a first movement in translation T1 of the deformation part 104 along the axis X103 from its first position towards its intermediate position in which the central portion 142 of the cap 141 faces the central portion 183, the portion 183 thus being held between the cap 141 and the face 133A. This first movement in translation T1 of the deformation part 104 is actuated by turning the lever 105 through a first angle in the direction of arrow R1 in
Once the central portion 183 of the bridge 108 is held in this way relative to the receiver portion 133, the branches 107 of the staple 106 are inserted into the bores 191. In particular, the distal end 171 of each branch 107 is positioned facing a respective bore 191 and a thrust force is exerted on the proximal portion 139 of the main body 103 so that each branch 107 penetrates into the corresponding bore 191 until a front face 182 of the bridge 108 that faces towards the branches 107 comes into contact with the surfaces of the bone portions 9.
Once the branches 107 have been maximally inserted in the bores 91, the staple 106 is deformed to put the bone portions 9 into compression. For this purpose, the deformation part 104 is actuated to perform a second movement in translation T2 along the axis X103 from its intermediate position towards its second position as shown in
The movement of the distal ends 171 of the branches 107 towards each other during deformation of the staple 106 then generates a force urging the bone portions 9 towards each other, thereby enabling the surfaces of the two bone portions in the site F to be pressed one against the other with a certain amount of pressure. Because of the mechanical properties of the material constituting the staple 106, the branches 107 continue to converge in spite of the reaction force exerted by the wall of each bore 91 against the corresponding branch.
After the staple 106 has been deformed in this way, the receiver portion 133 of the instrument 102 is separated from the staple 106 by actuating the deformation part 104 to move in translation T3 along the axis X103 from its second position towards its first position so as to release the bridge 108 from the cap 141, and then by removing the staple from the peg 134. The movement in translation T3 is actuated by turning the lever 105 in the direction of arrow R3 in
According to such embodiment, the staple-fitter assembly 101 enables compression to be applied to the bone portions 9 while the staple 106 is (e.g. maximally) engaged in the bone, e.g. while the bridge 108 of the staple is in contact with the surface of the bone. The mechanism for preventing the central portion 183 of the bridge of the staple from moving relative to the receiver portion does not act on the side of the bridge that faces towards the branches 107, and the tabs 143 of the deformation part 104 cooperate with the end portions 185 solely on the side of the bridge that is remote from the branches. Under such circumstances, it is possible to deform the staple 106 while it is fully impacted into the bone, thereby eliminating the need to perform two impacting operations in succession on the staple, one before and the other after deformation of the staple. This makes the staple easier to implant, and significantly reduces the time required for implanting it, according to embodiments of the present invention.
Furthermore, the instrument 102 enables the compression load applied to the bone portions 9 by the compression staple 106 to be controlled. It is possible to apply a controlled amount of thrust force P on the end portions 185 of the bridge 108 of the staple so as to generate an appropriate amount of deformation of the staple. In particular, the force P may be adjusted by varying the angle of rotation R2 of the lever 105, thus enabling the deformation part 104 to be driven in translation to a greater or lesser extent towards the bridge of the staple positioned on the receiver portion 133. This controlled deformation of the staple 106, and indeed that of the staple 6, differs from the deformation that is obtained with known staple-fitter assemblies that make use of compression staples made of shape memory material. For such staples made of shape memory material, the compression load applied to the bone portions for consolidating is imposed by the characteristics of the shape memory material, and there is no way of controlling it while the staple is being implanted. In addition, a compression staple of a staple-fitter assembly according to an embodiment of the present invention, e.g. made of stainless steel or of titanium, is less likely to give rise to allergic reactions than is a staple made of a shape memory material, and it does not put temperature constraints on its storage and its use. A compression staple of a staple-fitter assembly according to an embodiment of the invention, e.g. made of stainless steel or of titanium, can also be fabricated easily, with limited fabrication costs.
Embodiments of the present invention include various alterations and/or variations of the instrument 102 and the associated staple 106. For example:
Some embodiments of the present invention include one or more alterations and/or variations that applicable to staple 6 and staple 106. For example:
Various modifications and additions can be made to the exemplary embodiments discussed without departing from the scope of the present invention. For example, 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. For example, while the embodiments described above refer to particular steps, the scope of this invention also includes embodiments having different combinations of steps and embodiments that do not include all of the described steps. 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.
| Number | Date | Country | Kind |
|---|---|---|---|
| 08 58093 | Nov 2008 | FR | national |