Surgical shoulder articulation replacement method
10898348 ยท 2021-01-26
Assignee
Inventors
Cpc classification
A61F2002/4663
HUMAN NECESSITIES
A61F2/30942
HUMAN NECESSITIES
A61F2002/30616
HUMAN NECESSITIES
A61F2002/30718
HUMAN NECESSITIES
A61F2/4657
HUMAN NECESSITIES
A61F2/30771
HUMAN NECESSITIES
A61F2002/30617
HUMAN NECESSITIES
A61F2/4003
HUMAN NECESSITIES
A61F2002/4687
HUMAN NECESSITIES
A61F2002/4681
HUMAN NECESSITIES
International classification
A61B17/17
HUMAN NECESSITIES
Abstract
A surgical shoulder articulation replacement method is provided. The method can include providing a humeral implant having a hollow stem. The hollow stem can be provided with a sharp distal edge. The method can include impacting the humeral implant in a cancellous bone of a humeral head of a patient, with the sharp distal edge cutting the cancellous bone in the process.
Claims
1. A surgical shoulder articulation replacement method comprising: a) providing a humeral implant having a hollow stem, said hollow stem being provided with a sharp distal edge comprising a non-circular continuous periphery, b) making a reference mark comprising a non-circular continuous periphery on a cancellous bone of a humeral head of a patient, the reference mark corresponding to the desired location of impaction of the sharp distal edge of the hollow stem; c) aligning the non-circular continuous periphery of the sharp distal edge of the hollow stem with the non-circular continuous periphery of the reference mark; d) impacting the humeral implant in the cancellous bone of the humeral head of the patient at the desired location of impaction, with the sharp distal edge cutting the cancellous bone in the process.
2. Surgical method according to claim 1, wherein it further comprises a step comprising attaching an articulation member on the humeral implant.
3. Surgical method according to claim 1, wherein it comprises a further step, prior to step a), comprising determining the size and shape of the humeral implant using imaging.
4. Surgical method according to claim 3, wherein the size and shape of the humeral implant are determined using a CT scan or MRI.
5. Surgical method according to claim 1, wherein it comprises a step comprising providing an insertion guide adapted to guide the impaction of the humeral implant.
6. Surgical method according to claim 1, wherein prior to step b), the method comprises a step comprising making a cut in a cortical bone of the humeral head so as to uncover the cancellous bone.
7. Surgical method according to claim 1, wherein it comprises a further step comprising holding the humeral implant with a holding tool fixed to the humeral implant and having a handle.
8. Surgical method according to claim 7, wherein it comprises a further step comprising impacting the holding tool with a striking instrument.
9. Surgical method according to claim 1, wherein it comprises a further step comprising impacting the humeral implant with a striking instrument.
10. Surgical method according to claim 1, wherein it comprises a further step comprising impacting a detachable portion of the humeral implant with a striking instrument, then removing the detachable portion once the humeral implant is at its final place in the bone.
11. Surgical method according to claim 1, wherein it comprises a further step comprising providing a set of humeral implants of different sizes and shapes.
12. Surgical method according to claim 1, wherein the hollow stem has an ovoid cross section.
13. Surgical method according to claim 1, wherein the hollow stem of the humeral implant is pierced with transversal holes.
14. Surgical method according to claim 1, wherein the humeral implant is made by additive manufacturing.
15. Surgical method according to claim 1, wherein the humeral implant is manufactured in titanium or titanium alloy.
16. Surgical method according to claim 1, wherein the reference mark is provided by a reference punch matching the shape of the sharp distal edge of the hollow stem and adapted to create a groove in the bone.
17. A surgical shoulder articulation replacement method comprising: a) determining the size and shape of a humeral implant using imaging, b) providing the humeral implant with a hollow stem, said hollow stem having a sharp distal edge comprising a periphery, c) making a reference mark comprising an oblong continuous periphery on a cancellous bone of a humeral head of a patient, the oblong continuous periphery of the reference mark matching at least a portion of the periphery of the sharp distal edge of the hollow stem, the reference mark corresponding to the desired location of impaction of the sharp distal edge of the hollow stem; d) impacting the humeral implant in the cancellous bone of the humeral head of the patient at the desired location of impaction, with the sharp distal edge cutting the cancellous bone in the process.
18. Surgical method according to claim 17, wherein the hollow stem has an ovoid cross section.
19. A surgical shoulder articulation replacement method comprising: a) providing a humeral implant having a hollow stem and a mounting surface comprising a mounting hole, said hollow stem being provided with a sharp distal edge and an interior channel, the mounting hole of the humeral implant being in communication with the interior channel of the hollow stem to provide an open passage from a proximal end of the humeral implant to a distal end of the humeral implant; b) impacting the humeral implant in a cancellous bone of a humeral head of a patient, with the sharp distal edge cutting the cancellous bone in the process.
20. Surgical method according to claim 19, wherein the hollow stem has a circular cross section.
Description
(1) The invention will now be explained in reference to the annexed drawings, as an illustrative example. In the annexed drawings,
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(16) As represented on
(17) In an embodiment, the method further comprises a pre-op planning/imaging step, which is operated prior to the step of providing the humeral implant 2 and which consists of determining the size and shape of the implant 2 using imaging. The imaging may include CT scans, MRI or any other convenient imaging technique. In one embodiment, the implant may have a radius of curvature (along a longitudinal axis), which is determined in the pre-op planning/imaging.
(18) In an embodiment, the humeral implant 2 may be made by additive manufacturing. This allows providing the humeral implant 2 with a non-tubular shape, for example a curved hollow shape as represented on the figures, or any other shape determined on the basis of the shape of the humeral head of the patient. For example, the implant may be manufactured by metal powder bed fusion technologies.
(19) Of course, other manufacturing processes may be considered for obtaining the humeral implant 2.
(20) In an embodiment, the humeral implant 2 is manufactured in titanium or titanium alloy.
(21) In an embodiment, the humeral implant 2 may be manufactured in its final shape in a single operation. The implant 2 does not need complementary machining operations to obtain its final shape.
(22) The method may provide to provide a set of humeral implants 2 of different sizes and shapes. The surgeon may choose between the different sizes and shapes depending on the shape and size of the humeral head 1 of the patient determined by imaging techniques.
(23) Alternatively, the humeral implant 2 may be patient-specific sized and shaped and directly manufactured in its patient-specific final state by additive manufacturing, to best fit to the shoulder articulation of the patient.
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(25) The method may consist of impacting the humeral implant 2 with a non-shown striking instrument, such as a hammer, by striking the implant 2 directly on the articulation surface 6.
(26) In an alternative optional embodiment represented on
(27) In an embodiment, the method may consist of impacting the holding tool 8 with a non-shown striking instrument, such as a hammer. The holding tool 8 may comprise a flat top surface 84 provided for striking the holding tool 8 with a hammer.
(28) In an optional embodiment, the method may consist of impacting a detachable portion 9 of the humeral implant 2 with a striking instrument, then removing the detachable portion 9 once the humeral implant 2 is at its final place in the bone. The detachable portion 9 may be, for example, a part manufactured together with a main body of the humeral implant, or another part mounted on the mounting surface 6 and provided to protect the mounting surface 6 during transport and/or impaction.
(29) In an embodiment, the method further comprises a step consisting of attaching the non-shown articulation member on the mounting surface 6 of the humeral implant 2.
(30) Prior to impacting the humeral implant 2 in the humeral head 1, the method may comprise a step consisting of making a cut in a cortical bone portion 1b of the humeral head 1, so as to uncover the cancellous bone 1c, and provide a flat resected surface 1a.
(31) In a non-shown embodiment; the hollow stem 4 of the humeral implant 2 may be pierced with transversal holes. The cancellous bone 1c may get inside the interior channel 40 during impaction of the humeral implant 2 via the transversal holes.
(32) In an embodiment, the hollow stem 4 may have a circular cross-section or an ovoid cross-section.
(33) As represented on the figures, the humeral implant 2 may have an increasing transversal section from the sharp distal edge 42 to the mounting surface 6. In non-shown alternatives, the transversal section of the humeral implant 2 may have different progression profiles.
(34) In some embodiment, the method may comprise a step consisting of providing an insertion guide 3 adapted to guide the impaction of the humeral implant 2. Such insertion guide 3 may include, for example, an insertion window Win which the humeral implant 2 is inserted during impaction so that the humeral implant 2 follows the right path for the intended final position of the humeral implant 2.
(35) In an optional embodiment represented on
(36) To this end, a positioning tool 10, represented on
(37) From the inferior surface 124 extends a protrusion 126 provided with a lateral contour 126a that is complementary to the shape of the hole 104. From the protrusion 126 extends an impacting body 128 which is formed by a tube having a transversal section matching the transversal section of the hollow stem 4 of the humeral implant 2. As represented on
(38) In an alternative embodiment represented on
(39) The method allows providing a lighter humeral implant for the patient, due to the hollow feature of the humeral implant. The hollow feature of the humeral implant also allows savings on raw materials and weight of shipments.
(40) The insertion of the cancellous bone 1c into the interior channel 40 allows cancellous bone preserving and a non-invasive technique.
(41) The direct impaction of the humeral implant 2 in the cancellous bone allows time saving in operation room, as time for bone preparation is greatly reduced. The direct impaction also allows cost reduction on expensive patient-specific or ranges of compactor, rasps and cutting guides, and subsequent shipment weight and costs.
(42) The use of additive manufacturing techniques allows savings on post machining operations, and makes possible specific implant shapes.