Method of osteosyntheses or arthrodesis of two-bone parts, in particular of the hand and / or foot
10022167 ยท 2018-07-17
Assignee
Inventors
- Marc Augoyard (Tassin la Demi Lune, FR)
- Jacques Peyrot (Tassin la Demi Lune, FR)
- Tristan Meusnier (Saint-Etienne, FR)
- Bernard Prandi (Rennes, FR)
Cpc classification
A61B17/7291
HUMAN NECESSITIES
A61F2002/30622
HUMAN NECESSITIES
A61B17/68
HUMAN NECESSITIES
A61F2002/30092
HUMAN NECESSITIES
A61B17/7258
HUMAN NECESSITIES
A61F2210/0019
HUMAN NECESSITIES
A61B17/844
HUMAN NECESSITIES
International classification
A61B17/84
HUMAN NECESSITIES
Abstract
In one embodiment, the present invention is a fixation device including a median zone having a substantially triangular shape; a first fixation zone including first and second tabs that, in a separated configuration, extend away from each other from an end of the median zone, the first fixation zone having a first region adjacent the median zone and a second region adjacent the first region. Also, within the first region of the first fixation zone, an inner surface of each of the first and second tabs of the first fixation zone extends outwardly and proximally from the median zone to a first point to form an arch, and from the first point, the inner surface of each of the first and second tabs extends toward a second point. Further, within the second region of the first fixation zone, the inner surface of each of the first and second tabs of the first fixation zone extends outwardly from each second point to a respective third point so that the inner surface of each of the first and second tabs from the second point to the third point is arcuate and convex.
Claims
1. A fixation device comprising: a median zone having a substantially triangular shape; a first fixation zone including first and second tabs that, in a separated configuration, extend away from each other from an end of the median zone, the first fixation zone having a first region adjacent the median zone and a second region adjacent the first region; wherein, within the first region of the first fixation zone, an inner surface of each of the first and second tabs of the first fixation zone extends outwardly and proximally from the median zone to a first point on each of the first and second tabs to form an arch extending continuously from the first point on the first tab to the first point on the second tab, and from each of the first points, the inner surface of each of the first and second tabs extends toward a second point, and within the second region of the first fixation zone, the inner surface of each of the first and second tabs of the first fixation zone extends outwardly from each second point to a respective third point so that the inner surface of each of the first and second tabs from the second point to the third point is arcuate and convex.
2. The device of claim 1, wherein each tab in a first fixation zone includes at least one outwardly projecting barb adapted to engage bone, the barb including a decline toward the distal end of the fixation device.
3. The device of claim 1, further comprising a generally rectangular connecting zone adjacent the median zone.
4. The device of claim 1, further comprising a second fixation zone including first and second tabs extending outwardly in a proximal direction away from a distal tip.
5. The device of claim 4, wherein the second fixation zone is positioned at one end of the median zone and the first fixation zone is positioned at an opposite end of the median zone, wherein both the first and second tabs of the second fixation zone and the first and second tabs of the first fixation zone extend proximally.
6. The device of claim 1, wherein the first and second tabs of the first fixation zone comprise a first width in the separated position.
7. The device of claim 6, wherein the first and second tabs of the first fixation zone comprise a second width in an implantable position that is narrower than this first width.
8. The device of claim 4, wherein the first and second tabs of the second fixation zone have a first width in an open position.
9. The device of claim 8, wherein the first and second tabs of the second fixation zone have a second width in an implantable position that is narrower than the first width.
10. A fixation device comprising: a body extending between a proximal end and a distal end including a proximal fixation zone, a distal fixation zone and a median zone positioned between the proximal and distal fixation zones, the proximal fixation zone including a first tab and a second tab that, in a separated zone, extend from a proximal end of the median zone in a radially outward direction to a first tab end and a second tab end, wherein an inner surface of the first and second tabs forms a first length extending from adjacent the median zone to a first point on each of the first and second tabs with an increasing slope along the first length, forms a second length along each of the first and second tabs with a decreasing slope from the first point to a second point, and forms a third length along each of the first and second tabs with an increasing slope from the second point to the respective first tab end and second tab end.
11. The device of claim 10, wherein the decreasing slope from the first point to the second point defines a concave surface.
12. The device of claim 10, wherein the increasing slope from the second point to the first and second tab ends defines a convex surface.
13. The device of claim 10, wherein the first tab end and second tab end each form an apex of each of the first and second tabs and, from the apex, the inner surface of each tab extends to a barb positioned on an outer surface of each of the first and second tabs.
14. The device of claim 10, wherein the distal fixation zone includes a first tab and a second tab extending in a radially outward direction from a distal-most end towards the median zone.
15. The device of claim 14, wherein the first and second tabs of the proximal fixation zone and the first and second tabs of the distal fixation zone both extend radially outwards in a proximal direction.
16. The device of claim 15, further comprising a generally rectangular connecting zone positioned between the median zone and the distal fixation zone.
17. A fixation device comprising: a monolithic body extending between a proximal end and a distal end including a proximal fixation zone, a distal fixation zone and a median zone positioned between the proximal and distal fixation zones, the proximal fixation zone including a first tab and a second tab, the first and second tabs each having a first region adjacent a second region, and the distal fixation zone including a first tab and a second tab extending in a radially outward direction from a distal-most end towards the median zone, wherein the proximal fixation zone has an open position, in the open position an inner surface of the first region of the first and second tabs forms a convex surface and an inner surface of the second region of the first and second tabs forms a concave surface.
18. The fixation device of claim 17, wherein the proximal fixation zone has an implantable position, in the implantable position the inner surface of the second region of the first and second tabs is substantially linear.
19. The fixation device of claim 17, wherein the convex surface is proximal to the concave surface.
20. The fixation device of claim 17, wherein the inner surface of the first region of the first and second tabs forms an arch.
Description
BRIEF DESCRIPTION OF THE DRAWING
(1) The invention is described below in greater detail in conjunction with the figures of the drawings appended hereto in which:
(2)
(3)
(4)
(5)
SPECIFIC DESCRIPTION
(6) The arthrodesis element of the invention consists of an elongated body 1. Each of the ends of the body 1 is conformed to produce a fixation zone 1a linked to a fixation zone 1b.
(7) Between the two fixation zones 1a and 1b, at least one median zone 1c is formed capable of withstanding shear and bending stresses. In general, the shear and bending stresses are applied to the bone site to be consolidated. The shape of this median zone 1c is adapted to the internal shape of the bone. Its length is determined in order to allow a slight offset in the centering.
(8) For information, and in a non-limiting manner, this median zone may have a rectangular cross-section measuring about 2 to 3 mm*1 to 1.5 mm and a length of about 3 to 5 mm for the foot and the hand.
(9) The fixation zones 1a and 1b are conformed to prevent any rotational movement, resist tension, and maintain manual compression applied at the time of the implant by the surgeon in order to reduce the site. To obtain this result, the fixation zones 1a and 1b are made from a shape-memory material to be deformed by thermal action (tepid memory) or mechanical action (superelasticity) (see U.S. Pat. No. 5,958,159). The goal, in the fixation zones, considering their profile on the one hand and the type of material on the other, is to permit an introduction into the bone parts, particularly dorsally without a finger- or toe-tip approach, on the one hand, and to produce a fixation in the bone portion in order to obtain or to maintain the desired compressive force, on the other. The fixation zones 1a and 1b are identical or not, according to the type of bone and its morphology.
(10) Depending on the type of arthrodesis performed, that is, the type of interphalangeal joint to be consolidated for example, the fixation zones 1a and 1b may have different embodiments.
(11) For example, one of the fixation zones 1a has two tabs or wings that are separable under a thermal action for example. Otherwise, these fixation zones 1a may have a single tab or rod which can be curved under the action of a memory of the component material. Otherwise, the fixation zone 1b has, in its thickness, a slot to permit deformation by elasticity, under thermal action for example, and to maintain the position by pressing on the length of the bone.
(12) According to another feature of the invention, to take account of the anatomy of the various phalanges for example, that is the internal shrinkage of the bone (hourglass shape), the median zone 1c is linked to at least one of the fixation zones 1b by a thinner connecting zone 1d.
(13) Reference can be made to the figures of the drawings which show an embodiment of an intramedullar arthrodesis element.
(14) In this embodiment, the body 1 has, at one of its ends, a fixation zone 1a in the form of two tabs or wings 1a1 1a2. This fixation zone 1a is prolonged by a median zone 1c of generally substantially triangular shape in a plan view. The median zone 1c is connected to the other end fixation zone 1b by a connecting zone 1d having a generally rectangular shape in a plan view. The fixation zone 1b has, in its thickness, a slot of generally oblong shape 1b1.
(15) Reference can be made to
(16) It should be noted that the profile of the median zone 1c prevents penetration when the site is reclosed.
(17) In an alternative embodiment, the connecting zone 1d can be split to benefit from a swelling effect by shape memory and strengthening of the anchoring in the diaphyseal zone.
(18) It should be recalled that the inventive element is ideal for the treatment of the hammer- or claw-toe syndrome, by performing an arthrodesis in the phalanges P1 and P2 on the radii 2 to 5, while observing that such applications must not be considered as limiting, by means of essentially dimensional adjustments (finger reimplants, arthrodesis of the distal interphalangeal joint and of the proximal interphalangeal joint of the hand, and the arthrodesis of the big toe).
(19) Obviously, the entire arthrodesis element of the invention may have constructive features suitable for improving the fixation and compression in particular.
(20) For example:
(21) notches on the tabs on one of the sides for better fixation in the ethmoid bone;
(22) wavy tabs implanted (straight before implant)
(23) to permit shortening and hence an additional compression of the arthrodesis site compared with a simple fixation;
(24) a tapered central zone to avoid undesirable
(25) penetration of the implant at the time when the site is to be closed.
(26) For information, the memory used is preferably a tepid memory, so that heating is unnecessary because of the lack of access. The opening begins at above 15 to 20 C. and stops at about 30 to 35 C.
(27) The operating technique remains conventional.