Artificial knee joint
11033397 · 2021-06-15
Assignee
Inventors
- Young-Woong Jang (Seoul, KR)
- Chan-Eol Kim (Seoul, KR)
- Jae-Hun Ro (Seoul, KR)
- Ah-Reum Han (Gangwon-do, KR)
- Myung-chul LEE (Gyeonggi-do, KR)
- Yong In (Seoul, KR)
- Seung-Beon Han (Seoul, KR)
Cpc classification
A61F2/3886
HUMAN NECESSITIES
A61F2002/30001
HUMAN NECESSITIES
A61F2002/30878
HUMAN NECESSITIES
A61F2002/30884
HUMAN NECESSITIES
International classification
Abstract
An artificial knee joint includes a tibial component implanted into the proximal end of a tibia, and a bearing component coupled to the tibial component, in which the tibial component includes an interference prevention portion capable of preventing interference with the bearing component when the bearing component is inserted diagonally and the bearing component includes a protrusion coupled to the interference prevention portion.
Claims
1. An artificial knee joint comprising: a tibial component configured to be implanted into a proximal end of a tibia, the tibial component comprising: a base plate including a rim protruding along a peripheral edge; and invagination recesses recessed in the rim across an M-L line of the tibial component on both a lateral side and a medial side; and a bearing component configured to be coupled to the tibial component; each of the invagination recesses including one end and a remaining end, the one end located at a posterior side of the M-L line and the remaining end located at an anterior side of the M-L line, such that the invagination recesses prevent interference of the tibial component with the bearing component during insertion thereof in an oblique direction with respect to the bearing component.
2. The artificial knee joint of claim 1, wherein the invagination recesses are provided symmetrically with reference to an A-P line.
3. The artificial knee joint of claim 1, wherein the bearing component includes a protrusion configured to be coupled to the invagination recesses, the protrusion extending downward from a periphery of the bearing component corresponding to a position of the invagination recesses formed in the tibial component.
4. The artificial knee joint of claim 3, wherein the protrusion has a shape complementary to a shape of the invagination recesses.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The above and other aspects, features and advantages of the present disclosure will be more apparent from the following detailed description taken in conjunction with the accompanying drawings, in which:
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DETAILED DESCRIPTION OF THE EXEMPLARY EMBODIMENTS
(14) Hereinafter, an artificial knee joint of the present disclosure will be described in detail with reference to the accompanying drawings. It is to be noted that the same elements among the drawings are denoted by the same reference numerals if possible. In the following description, s detailed description of well-known functions or constructions will be omitted when it may make the subject matter of the present disclosure rather unclear. Unless defined otherwise, all terms used herein have the same meaning as the general meaning of the terms understood by a person ordinarily skilled in the art to which this disclosure belongs and, when the general meaning conflicts with the meaning of the terms used herein, the meaning of the terms follows the definition used in the specification.
(15) In this application, with reference to the coronal plane, “A” indicates the anterior side to which the face of the person is directed and “P” indicates the posterior side to which the rear portion of the head of the person is directed. With reference to the sagital plane, “M” indicates the medial side and “L” indicates the lateral side.
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(17) The tibial component 3 is inserted into the upper side of the tibia and the bearing component 5 is received in the upper side of the tibial component 3 and coupled to the bearing component 5 so as to form a predetermined shape that forms a portion of the tibial component. For this purpose, the tibial component 3 includes a stem 31 and a base plate 33.
(18) The stem 31 is inserted into the patient's tibia in artificial knee joint operation, and may be generally classified into a bone-cement-fixing type for improving the bonding strength between the tibia and the stem 31 and a cementless type in which bond cement is not used. The stem 31 may have other various structures for fixing the stem 31 at the medial side of the tibia.
(19) The base plate 33 is a portion on which the bearing component 5 is seated, and includes a plate bottom 331 and a rim 332. The base plate 33 is generally made of a single metal such as a Ti alloy or a CoCr alloy. When a lamination technique is used, it is possible to make the plate bottom 331 and the rim 332 using different materials.
(20) The rim 332 is erected on the plate bottom 331, and below the plate bottom, there is a bonding surface between the base plate 33 and the stem 331, in which the lower portion of the plate bottom 331 and the upper end surface of the stem are bonded to each other, so that the base plate 33 and the stem 31 are coupled to each other.
(21) The rim 332 protrudes upwards along the lateral peripheral edge of the plate bottom 531 so as to define a coupling space in which the bearing component 5 of the artificial knee joint is seated. The rim 332 may be customized to have different shapes, heights, and sizes depending on the patient, and may include a posterior protrusion 3321, an anterior recess 3322, and invagination recesses 3323.
(22) The posterior protrusion 3321 is bent at the rim 332 so as to extend in the horizontal direction, and is inserted into and engaged in a coupling groove 531 in the bearing component 5. Such a coupling relationship is shown in
(23) The anterior recess 3322 is a portion formed in the process of bending the posterior protrusion 3321 to extend in the horizontal direction, and has a cross section of a letter “⊏” shape. Elastic hooks 532 of the bearing component 5 are inserted into and elastically engaged with the anterior recess 3322. Such a coupling relationship is shown in
(24) As shown in
(25) According to another embodiment of the present disclosure, invagination recesses 3323 are formed in a pair on the medial side M and the lateral side L of the rim of the base plate to be symmetrical to each other. It is not excluded that the intervals or the positions may be formed asymmetrically. For example, the invagination recesses of the medial side M and the invagination recesses of the lateral side L may be formed at different intervals, or the interval of the invagination recesses located in the insertion side may be longer than the interval of the invagination recesses located opposite thereto.
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(27) Referring to
(28) The post 511 protrudes upwards from one side of the upper surface of the bearing component 5. Artificial knee joint operations include a Cruciate-Retaining-type (CR-type) operation and a Posterior-Stabilized-type (PS-type) operation. The CR-type operation is an artificial knee joint operation which is performed in the state in which the posterior cruciate ligament is not removed, and the PS-type operation is an artificial knee joint operation, in which the posterior cruciate ligament is replaced with the post 511 of the bearing component 5 in the state in which the posterior cruciate ligament is removed. In the case of the PS-type artificial knee joint operation, the post 511 of the bearing component 5 and the cam of the femur insertion member replaces the removed posterior cruciate ligament. Accordingly, the post 511 is a structure necessary for the artificial knee joint operation when the posterior cruciate ligament is removed. The post 511 is not an essential structure of the present disclosure, but may be included in the bearing component 5 depending on a surgical operation.
(29) The groove 512 extends to the lower end of the post 511, and provides a joint surface that is in contact with the femur insertion member (not shown) so as to allow the joint surface to perform joint motion.
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(31) The coupling recess 531 is a portion invaginated in the rear surface of the bearing component 5, i.e., at the posterior side P such that during coupling with the tibial component 3 the posterior protrusion 3321 of the tibial component 3 is inserted into the coupling recess 531, thereby forming a firm coupling. Such a coupling relationship is shown in
(32) The elastic hook 532 protrudes from the front surface of the bearing component, that is, toward the anterior side A. During the coupling with the tibial component 3, the elastic hook 532 is inserted into the anterior recess 3322 of the tibial component 3, thereby forming a firm coupling. Such a coupling relationship is shown in
(33) The side portion 55 is a portion that connects the upper portion 31 and the lower portion 53, and includes the protrusions 551 that form the periphery of the bearing component 5.
(34) The protrusions 551 are portions protruding downwards from the side portion 55 of the bearing component 5 and have a shape complementary to that of the invagination recesses 3323 in the tibial component 3. As described above, in the process of performing a minimally invasive knee joint replacement operation, the coupling position of the bearing component 5 may be aligned after being inserted into the tibial component 3 in the oblique direction in some cases due to a limitation resulting from the minimization of the skin incision portion. However, according to the present disclosure, the invagination recesses 3323 of the tibial component is capable of guiding coupling at the correct position by receiving the protrusions 551. In addition, since the protrusions 551 in the bearing component 5 and the invagination recesses 3323 in the tibial component 3 are coupled to each other with complementary shapes, the rotation of the bearing component 5 due to the motion of the artificial knee joint can be prevented so that the it is possible to maintain the position of the bearing component 5. Furthermore, since the coupling between the protrusions 551 and the invagination recesses 3323 is made without any gap, it is possible to prevent side effects such as the surrounding tissues being caught in a coupling gap in the recovery process after the operation process is terminated.
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(37) The foregoing detailed description illustrates the present disclosure. In addition, the foregoing description is intended to illustrate and explain embodiments of the present disclosure, and the present disclosure may be used in various other combinations, modifications, and environments. That is, it is possible to change or modify the present disclosure within the scope of the concept of the present disclosure disclosed in this specification, within the scope equivalent to the above-described contents, and/or within the scope of the skill or knowledge of a person skilled in the art. The embodiments described above are intended to illustrate the best mode for carrying out the technical idea of the present disclosure, and various modifications required for specific applications and uses of the present disclosure are also possible. Therefore, the detailed description of the present disclosure is not intended to limit the present disclosure to the disclosed embodiments. In addition, the appended claims should be interpreted as covering other embodiments as well.