FR2502939A1 - ROD WITH DEVICE FOR ANCHORING A STENT IN OR ON A BONE - Google Patents
ROD WITH DEVICE FOR ANCHORING A STENT IN OR ON A BONE Download PDFInfo
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- FR2502939A1 FR2502939A1 FR8206309A FR8206309A FR2502939A1 FR 2502939 A1 FR2502939 A1 FR 2502939A1 FR 8206309 A FR8206309 A FR 8206309A FR 8206309 A FR8206309 A FR 8206309A FR 2502939 A1 FR2502939 A1 FR 2502939A1
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- Prior art keywords
- bone
- rod
- prosthesis
- anchoring
- bars
- Prior art date
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Links
- 210000000988 bone and bone Anatomy 0.000 title claims abstract description 61
- 238000004873 anchoring Methods 0.000 title claims description 16
- 238000010348 incorporation Methods 0.000 claims description 2
- 230000000638 stimulation Effects 0.000 claims description 2
- 239000002639 bone cement Substances 0.000 abstract description 8
- 239000007943 implant Substances 0.000 abstract 1
- 230000035764 nutrition Effects 0.000 abstract 1
- 235000016709 nutrition Nutrition 0.000 abstract 1
- 230000000717 retained effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 description 6
- 230000006835 compression Effects 0.000 description 5
- 238000007906 compression Methods 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 238000002513 implantation Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 230000011164 ossification Effects 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 208000003322 Coinfection Diseases 0.000 description 1
- 206010020565 Hyperaemia Diseases 0.000 description 1
- 238000011882 arthroplasty Methods 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 210000004394 hip joint Anatomy 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002784 sclerotic effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/32—Joints for the hip
- A61F2/36—Femoral heads ; Femoral endoprostheses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30721—Accessories
- A61F2/30724—Spacers for centering an implant in a bone cavity, e.g. in a cement-receiving cavity
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2/30771—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/28—Bones
- A61F2002/2821—Bone stimulation by electromagnetic fields or electric current for enhancing ossification
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/28—Bones
- A61F2002/2835—Bone graft implants for filling a bony defect or an endoprosthesis cavity, e.g. by synthetic material or biological material
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30316—The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30535—Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30579—Special structural features of bone or joint prostheses not otherwise provided for with mechanically expandable devices, e.g. fixation devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30316—The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30535—Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30602—Shaft made of a bundle of anchoring rods or bristles, e.g. fasciculate shaft
Landscapes
- Health & Medical Sciences (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Prostheses (AREA)
Abstract
Description
La présente invention concerne la tige d'une prothèse d'articulation et l'ancrage de celle-ci dans ou sur un os. Actuellement, la plupart des tiges de prothèse utilises sont de section transversale circulaire, quadrangulaire, en forme de lande ou de lemniscate. The present invention relates to the stem of a joint prosthesis and the anchoring thereof in or on a bone. Currently, most of the prosthesis stems used are of circular, quadrangular, heath or lemniscate cross section.
Dans la forme de section transversale, elles constituent un assemblage cohérent, non articulé. En outre la technique d'implantation comprend en principe deux procédés d'ancrage.In the form of cross section, they constitute a coherent, non-articulated assembly. In addition, the implantation technique in principle comprises two anchoring methods.
Suivant le premier procédé, qui est le plus fréquemment employé, l'ancrage est réalisé au moyen du système dénommé à ciment osseux" (systèmes Charnley, Charnîey-Mùller, Weber-Huggler et autres). Le ciment osseux est, dans son type le plus souvent utilisé, un polymethylmétacrylate, comme matière synthétique à deux composants. Lors de la polymérisation, il se produit par instant des températures élevées, non physiologiques, qui attaquent également partiellement l'os et parfois le détruisent. A beaucoup d'endroits, il est nécessaire que le ciment osseux assure la transmission des forces de la tige de prothèse à l'os. Il en résulte ici un double danger pour l'ancrage de la prothèse.D'une part, le ciment osseux qui est, de toute manière, le partenaire de plus faible résistance dans la liaison entre métal ciment osseux et os, subit souvent une introduction de sang lors de la mise en place par enfichage, de telle sorte que sa capacité de support se trouve réduite et qu'il se produit prématurément un fissurage du ciment sous l'effet d'une charge. D'autre part, la forme de lame ou forme polygonale de la section transversale implique des tensions de cisaillement extrêment élevées qui provoquent des fissures permanentes dans le ciment et finalement un relâchement de l'ancrage de la prothèse dans ou sur l'os du patient. According to the first process, which is the most frequently used, anchoring is carried out by means of the system known as bone cement "(Charnley, Charnîey-Miiller, Weber-Huggler and others systems). Bone cement is, in its type the more often used, a polymethylmetacrylate, as a two-component synthetic material. During polymerization, there occur instantaneously high temperatures, not physiological, which also partially attack the bone and sometimes destroy it. In many places, it It is necessary that the bone cement ensures the transmission of the forces from the prosthesis rod to the bone. This results in a double danger here for the anchoring of the prosthesis. On the one hand, the bone cement which is, in any case , the partner of weakest resistance in the bond between metal bone cement and bone, often undergoes an introduction of blood during the installation by plugging, so that its support capacity is reduced and that it occurs premature ment of a cracking of the cement under the effect of a load. On the other hand, the blade shape or polygonal shape of the cross section implies extremely high shear stresses which cause permanent cracks in the cement and ultimately loosening of the prosthesis anchor in or on the patient's bone. .
Enfin, des fentes capillaires formées entre le ciment osseux, la tige de prothèse et l'os, constituent un terrain favorable à la croissance de germes qui, d'après Buchholz, sont responsables d'infections secondaires profondes, aboutissant à un relâchement de l'ancrage de la prothèse. Finally, capillary slits formed between the bone cement, the prosthesis stem and the bone, constitute a favorable ground for the growth of germs which, according to Buchholz, are responsible for deep secondary infections, leading to a relaxation of the anchoring of the prosthesis.
Le second prodé, dénommé "ancrage sans ciment" doit éviter les risques mentionnés ci-dessus. On peut mentionner à ce sujet les prothèses constituées en céramique et métal avec un profil à nervures de support ou avec une structure de surface appropriée (d'après
Mittelmeier, Judet entre autres). Dans tous ces types de tiges d'ancrage de prothèse sans ciment, il peut se produire, entre la tige et l'os, des pointes de charge considérables, qui ont pour conséquence une résorption de l'os et ainsi un relâchement de l'ancrage. En outre, il est connu, depuis une demi-décade, et d'après de nombreuses études biomécaniques (Dornier/Rôhrle et autres notamment) que, dans le cas des tiges de prothèse et ancrages usuels, l'os est soumis à des sollicitations de caractère non physiologique.Lors d'une sollicitation trop élevée ou trop faible, d'après Wolff et autres, la constitution physiologique dé l'os est détruite. Une tige de prothèse qui transmet la force dans l'os suivant le principe physiologique de ceinturage de pression et de traction, ne provoque pas de tensions comparables à celles qui interviennent dans un os sain soumis à des charges.The second product, called "cementless anchoring" must avoid the risks mentioned above. Mention may be made in this connection of prostheses made of ceramic and metal with a profile with supporting ribs or with an appropriate surface structure (from
Mittelmeier, Judet among others). In all these types of cementless prosthesis anchor rods, considerable spikes can occur between the rod and the bone, which result in absorption of the bone and thus relaxation of the bone. anchoring. In addition, it has been known, for half a decade, and according to numerous biomechanical studies (Dornier / Rôhrle and others in particular) that, in the case of prosthesis rods and usual anchorages, the bone is subjected to stresses of a non-physiological character. When the stress is too high or too low, according to Wolff and others, the physiological constitution of the bone is destroyed. A prosthesis stem which transmits force into the bone according to the physiological principle of pressure and traction belts, does not cause tensions comparable to those which occur in healthy bone subjected to loads.
Dans la presque totalité des prothèses usuelles, on aboutit à une destruction sensible de l'os vivant, provoquée par l'obturation de l'extrémité osseuse, nécessitée par la construction même de la prothèse, ce qui peut également aboutir à un relâchement de l'ancrage. D'après les études micro-angio-graphiques de Rhînelander, l'effet Corticalis est principalement entretenu par la disposition histologique de la fermeture de l'extrémité de l'os. Cette dernière n'est d'ailleurs pas possible dans le cas de tiges de prothèse avec répartition uniforme de la charge sur grande surface, lorsque la tige remplit la totalité de l'espace libre de la moelle.In almost all common prostheses, there is a significant destruction of living bone, caused by the filling of the bone end, required by the construction of the prosthesis itself, which can also lead to loosening of the anchor. According to Rhînelander's micro-angio-graphic studies, the Corticalis effect is mainly maintained by the histological arrangement of the closure of the end of the bone. The latter is also not possible in the case of prosthesis rods with uniform distribution of the load over a large area, when the rod fills the entire free space of the cord.
En conséquence, l'invention a pour but de
ffi# réaliser une tige de prothèse avec ancrage de celle-ci sur ou dans un os, qui ne présente pas les inconvénients mentionnés ci-dessus. Plus particulièrement, l'ancrage doit pouvoir être réalisé sans le ciment osseux habituel, et doit assurer aussi bien une fixation primaire qu'une fixation permanente. Elle doit être compatible biologiquement, satisfaire du point de vue biomécanique aux exigences physiologiques, aussi bien lors du déplacement que dans le cas de charge permanente, et pouvoir être ancrée solidement et durablement à l'os. Elle doit ainsi simplement correspondre aux exigences d'une arthro-plastie à faible friction.Consequently, the object of the invention is to
ffi # make a prosthesis rod with anchoring thereof on or in a bone, which does not have the drawbacks mentioned above. More particularly, the anchoring must be able to be carried out without the usual bone cement, and must ensure both a primary fixation and a permanent fixation. It must be biologically compatible, meet the physiological requirements from a biomechanical point of view, both during movement and in the case of a permanent load, and be able to be anchored securely and durably to the bone. It must therefore simply meet the requirements of a low friction arthroplasty.
Dans ce but, l'invention est caractérisée en ce que la tige de prothèse est constituée par plusieurs barres individuelles qui permettent la transmission des forces, suivant le principe de ceinturage de traction et compression, sur la face physiologique de tension de traction et de compression de l'os, sans remplir complètement l'espace de la moelle. For this purpose, the invention is characterized in that the prosthesis rod is constituted by several individual bars which allow the transmission of forces, according to the principle of tension and compression belts, on the physiological face of tension of tension and compression of bone, without completely filling the space of the cord.
Grâce au domaine élastique, mais de forme stable, prévu dans la partie supérieure de la tige de prothèse, le ceinturage à la traction et à la pression est favorisé. Thanks to the elastic, but stable shape, provided in the upper part of the prosthesis stem, the belt under tension and pressure is favored.
Pour le raccordement à l'os, les barres individuellés sont pourvues d'une denture, ou d'une autre structure de surface connue dans la technique des implantations.For connection to the bone, the individual bars are provided with a toothing, or another surface structure known in the implantation technique.
Grâce à sa direction d'action, à sa forme, et à sa grandeur, on est assuré que les forces de traction et de pression dans la tige de prothèse, dues au poids du corps, à une force dynamique, ou à la traction de muscles, sont appliquées sur l'os, dans une mesure identique ou comparable aux tensions physiologiques dans un os normal.Thanks to its direction of action, its shape, and its size, it is ensured that the traction and pressure forces in the prosthesis stem, due to the weight of the body, to a dynamic force, or to the traction of muscles, are applied to the bone, to an extent identical or comparable to the physiological tensions in normal bone.
Pour la fixation primaire de la tige de prothèse, il est possible de mettre en oeuvre des chevilles ou douilles fixes, élastiques ou extensibles, ou éléments analogues, qui pressent les barres avec leur denture, ou leur structure superficielle, contre l'os, en s'accrochant dans celui-ci. Grâce à leur élasticité, les barres de la tige peuvent s'adapter largement à la forme particulière de l'os en question. De cette manière est assurée une transmission des forces sur une grande surface, ce qui évite une charge ponctuelle qui provoquerait une résorption. En outre, le processus de nourriture de l'os à partir de son extrémité, n'est pas sensiblement compromis, grâce à la forme en plusieurs membres de la tige. For the primary fixation of the prosthesis stem, it is possible to use fixed, elastic or extensible pins or sockets, or similar elements, which press the bars with their teeth, or their surface structure, against the bone, clinging to it. Thanks to their elasticity, the rod bars can largely adapt to the particular shape of the bone in question. In this way, a transmission of forces is ensured over a large area, which avoids a point charge which would cause absorption. In addition, the process of feeding the bone from its tip is not significantly compromised, thanks to the multi-member shape of the stem.
Une électrostimulation sert également à l'ancrage fixe de la tige de prothèse dans l'os. Il est connu que l'électrostimulation agit en trois phases, à savoir
Dans la phase initiale, il se forme, après une hyperemie primaire et une irrigation vasculaire accrue, un mésenchyme formateur de tissu osseux qui conduit à une angiofibromatose. Cette zone à formation osseuse suractivée constitue la zone enveloppe.Electrostimulation is also used for the fixed anchoring of the prosthesis rod in the bone. It is known that electrostimulation acts in three phases, namely
In the initial phase, after primary hyperemia and increased vascular irrigation, a bone tissue-forming mesenchyme is formed which leads to angiofibromatosis. This overactivated bone formation zone constitutes the envelope zone.
Dans la phase intermédiaire se produit le développement de tissu osseux sclérotique spongieux formateur de structure avec début d'insertion de calcium. In the intermediate phase there is the development of spongy sclerotic bone tissue that forms structure with the start of calcium insertion.
Dans la phase finale se produit un tissu osseux définitif, lamellaire, calcifié, orienté. Grâce à la forme spéciale et à la position de la cathode, autour de laquelle se forme le nouvel os, la tige de prothèse est entourée de tissu spongieux solide capable de supporter des forces. Ce tissu spongieux, causé par l'électro- stimulation est traversé par un réseau dense suffisant pour nourrir l'os. Pour favoriser la formation d'os et la fixation de la tige de prothèse, on introduit des copeaux d'os dans les espaces compris entre les douilles. In the final phase a definitive, lamellar, calcified, oriented bone tissue occurs. Thanks to the special shape and position of the cathode, around which the new bone is formed, the prosthesis stem is surrounded by solid spongy tissue capable of supporting forces. This spongy tissue, caused by electro-stimulation, is crossed by a dense network sufficient to nourish the bone. To promote bone formation and fixation of the prosthesis stem, bone chips are introduced into the spaces between the sockets.
L'invention est expliquée ci-après à l'aide d'exemples de réalisation avec d'autres caractéristiques, avec référence aux dessins annexés dans lesquels la figure 1 est une vue schématique en élévation latérale d'une endoprothèse avec tige à éléments groupés en faisceau, destinée à remplacer l'articulation de la hanche, insérée dans l'os d'entourage et adjonction d'un stimulateur électrique pour la formation d'os nouveau la figure 2 est une vue schématique en coupe à travers la tige de prothèse de la figure 1 et l'os qui l'entoure la figure 3 est une vue en élévation de la figure 1 en direction de la flèche A ; la figure 4 est une vue schématique d'une autre forme de réalisation d'une tige à deux éléments insérée dans l'os environnant la figure 5 est une vue en élévation en direction de la flèche B de la figure 4, la figure 6 est une vue en coupe de la tige de prothèse de la figure 4 la figure 7 est une vue en coupe schématique transversale d'une tige de prothèse suivant une autre forme de réalisation, comprenant ici trois barres et l'os environnant
Les figures 1 et 3 montrent une tige de prothèse d'un type nouveau qui se compose d'un faisceau de barres individuelles.La tige de prothèse peut être une seule pièce coulée, ou bien les barres individuelles (1, 2, 3 et 4) peuvent être fixées dans une collerette 5 (figure 3) au moyen de cones de serrage ou de filetages ou analogues Toutes les pièces peuvent etre en métal ou en un matériau complexe fibreux. L'articulation entre les barres individuelles 1 à 4 assure la transmission des forces dans l'os, suivant le principe de ceinturage à la traction et à la compression sur les côtés physiologiques de tension de traction 6 et de tension de compression 7 (figure 2) de l'os. Cela est favorisé par le domaine 8, dans une certaine mesure élastique, des barres 1 à 4. Pour leur raccordement à l'os 6, 7, les barres sont pourvues d'une denture 9, 10, ou d'une autre structure de surface connue dans la technique des implantations.Cette denture ou structure de surface est prévue de telle manière qu'elle soit efficace, sur la partie latérale 6 de l'os, contre une charge de traction, et sur la partie centrale de l'os 7, contre une charge de compression.The invention is explained below with the aid of exemplary embodiments with other characteristics, with reference to the appended drawings in which FIG. 1 is a schematic view in side elevation of a stent with rod with elements grouped in beam, intended to replace the hip joint, inserted into the surrounding bone and addition of an electric stimulator for the formation of new bone Figure 2 is a schematic sectional view through the prosthesis stem of Figure 1 and the bone surrounding it in Figure 3 is an elevational view of Figure 1 in the direction of arrow A; Figure 4 is a schematic view of another embodiment of a two-element rod inserted into the surrounding bone Figure 5 is an elevational view in the direction of arrow B in Figure 4, Figure 6 is a section view of the prosthesis stem of FIG. 4 FIG. 7 is a schematic transverse section view of a prosthesis stem according to another embodiment, here comprising three bars and the surrounding bone
Figures 1 and 3 show a new type of prosthesis rod which consists of a bundle of individual bars. The prosthesis rod can be a single cast, or the individual bars (1, 2, 3 and 4 ) can be fixed in a flange 5 (Figure 3) by means of clamping cones or threads or the like. All the parts can be made of metal or of a complex fibrous material. The articulation between the individual bars 1 to 4 ensures the transmission of the forces in the bone, according to the principle of belt under tension and under compression on the physiological sides of tension of tension 6 and of tension of compression 7 (figure 2 ) of the bone. This is favored by the domain 8, to a certain elastic extent, of the bars 1 to 4. For their connection to the bone 6, 7, the bars are provided with a toothing 9, 10, or another structure of surface known in the implantation technique This toothing or surface structure is provided in such a way that it is effective, on the lateral part 6 of the bone, against a tensile load, and on the central part of the bone 7, against a compression load.
Pour la fixation primaire de la prothèse, sont prévues des chevilles ou douilles élastiques 11, 12, 13, ou, comme représenté dans la figure 4, des douilles expansibles 24, qui pressent la denture 9, 10 des barres 1 à 4 dans la paroi 6, 7 de l'os et mettent en prise les dents ou la structure de surface. For the primary fixation of the prosthesis, elastic plugs or sleeves 11, 12, 13 are provided, or, as shown in FIG. 4, expandable sleeves 24, which press the teeth 9, 10 from bars 1 to 4 in the wall 6, 7 of the bone and engage the teeth or the surface structure.
Sous l'effet de la charge et de la stimulation électrique, il se forme un nouveau tissu osseux autour des barres 1 à 4. A partir du stimulateur 14, par un ou plusieurs câbles 25, les cathodes 15, 16, 17, 18 sont introduites dans 1 ì espace moelleux et disposées centralement ou dans toute autre position appropriée. L'anode 19 est raccordée par un câble séparé 20, au stimulateur électrique 14, et elle est fixée, avec un raccord de serrage 21 au trochanter principal. En vue d'accélérer la fixation de la prothèse, on introduit des fragments d'os dans la zone 8 et dans les espaces intermédiaires 22, 23 entre les douilles 11, 12 et 13. Under the effect of the charge and the electrical stimulation, new bone tissue is formed around the bars 1 to 4. From the stimulator 14, by one or more cables 25, the cathodes 15, 16, 17, 18 are introduced into 1 ì soft space and arranged centrally or in any other appropriate position. The anode 19 is connected by a separate cable 20, to the electrical stimulator 14, and it is fixed, with a clamping connection 21 to the main trochanter. In order to speed up the fixation of the prosthesis, bone fragments are introduced into the zone 8 and into the intermediate spaces 22, 23 between the sockets 11, 12 and 13.
A titre d'exemple, le signal du stimulateur 14 est délivré dans une fréquence de 38 à 43 Hertz, une durée de connexion de 30 à 58 % et un potentiel compris entre 300 et 900 millivolts. By way of example, the signal from the stimulator 14 is delivered in a frequency of 38 to 43 Hertz, a connection duration of 30 to 58% and a potential between 300 and 900 millivolts.
La figure 2 est une vue en coupe transversale de la constitution en forme de faisceau des barres individuelles 1, 2, 3 et 4. Le nombre et la grosseur des barres, ainsi que leur longueur, peuvent être choisi en fonction de la forme et du diamètre de l'os et de la charge. Figure 2 is a cross-sectional view of the beam-like construction of the individual bars 1, 2, 3 and 4. The number and size of the bars, as well as their length, can be selected depending on the shape and diameter of the bone and the load.
Les barres sont fixées de manière interchangeable dans la collerette 5 au moyen de cônes de serrage ou douilles de blocage connues de la technique.The bars are fixed interchangeably in the collar 5 by means of clamping cones or blocking sleeves known in the art.
Dans les figures 4, 5 et 6, la tige de prothèse est constituée par deux barres 1 et 2. Le groupement ou faisceau de la tige de prothèse commence directement à la sortie de la collerette 5. Comme variante à la réalisation de la figure 1, sont prévues ici quatre douilles expansibles 24 pour presser les barres 1, 2 contre l'os 6, 7. Comme il a été expliqué à propos de la figure 1, il est prévu, dans la tige de prothèse, une zone élastique 8. Les espaces intermédiaires 22, 23 entre les douilles expansibles 24, ainsi que la zone supérieure 8 de l'os sont remplis avec des fragments d'os, pour accélérer l'incorporation de la tige. In FIGS. 4, 5 and 6, the prosthesis rod is constituted by two bars 1 and 2. The grouping or bundle of the prosthesis rod begins directly at the outlet of the collar 5. As an alternative to the embodiment of FIG. 1 , four expandable sleeves 24 are provided here for pressing the bars 1, 2 against the bone 6, 7. As has been explained in connection with FIG. 1, an elastic zone 8 is provided in the prosthesis stem. The intermediate spaces 22, 23 between the expandable sleeves 24, as well as the upper zone 8 of the bone are filled with bone fragments, to accelerate the incorporation of the rod.
Dans la figure 7 est représentée une tige de prothèse composée de trois barres 1, 2, 3. In FIG. 7 is shown a prosthesis rod composed of three bars 1, 2, 3.
Claims (5)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19813113898 DE3113898A1 (en) | 1981-04-07 | 1981-04-07 | Stem and anchorage of an endoprosthesis in or on a bone |
Publications (1)
Publication Number | Publication Date |
---|---|
FR2502939A1 true FR2502939A1 (en) | 1982-10-08 |
Family
ID=6129501
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR8206309A Withdrawn FR2502939A1 (en) | 1981-04-07 | 1982-04-06 | ROD WITH DEVICE FOR ANCHORING A STENT IN OR ON A BONE |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE3113898A1 (en) |
FR (1) | FR2502939A1 (en) |
IT (1) | IT1192949B (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0086879A1 (en) * | 1982-02-23 | 1983-08-31 | GebràDer Sulzer Aktiengesellschaft | Clamp for centering the axially slidable shaft of an endoprosthesis inserted into a hollow bone |
FR2549717A1 (en) * | 1983-07-29 | 1985-02-01 | Cuilleron J | Femoral rod with flexible contacts for hip prosthesis |
WO1986006954A1 (en) * | 1985-05-23 | 1986-12-04 | Labor Für Experimentelle Chirurgie Schweizerisches | Self-locking stemmed component for a joint endo-prosthesis |
FR2610823A1 (en) * | 1987-02-12 | 1988-08-19 | Cuilleron J | Improved femoral rod for hip prostheses |
FR2628628A1 (en) * | 1988-03-15 | 1989-09-22 | Omci Sa | Femoral implant for hip replacement - comprises hollow conical shaft with gripping inserts pushed outwardly through peripheral opening by internal conical member |
EP0427902A1 (en) * | 1989-11-16 | 1991-05-22 | SULZER Medizinaltechnik AG | Rectilinear stam for hip joint prosthesis |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3843973A1 (en) * | 1988-12-27 | 1990-06-28 | Hermann Dr Med Kuenne | Total knee-joint endoprosthesis |
US5030236A (en) * | 1989-06-19 | 1991-07-09 | Intermedics Orthopedics, Inc. | Apparatus for enhancing biointegration of bony and endoprosthesis structures |
DE19544750A1 (en) * | 1995-11-30 | 1997-06-05 | Christoph Rehberg | Implantable device with internal electrode to promote tissue growth |
DE102005019546A1 (en) * | 2005-04-26 | 2006-11-09 | Didzun, Walter | Durable hip endoprosthesis shaft for implantation in humans |
DE102014108261A1 (en) | 2014-06-12 | 2016-01-07 | Universität Rostock | implant |
-
1981
- 1981-04-07 DE DE19813113898 patent/DE3113898A1/en not_active Withdrawn
-
1982
- 1982-04-06 FR FR8206309A patent/FR2502939A1/en not_active Withdrawn
- 1982-04-06 IT IT12498/82A patent/IT1192949B/en active
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0086879A1 (en) * | 1982-02-23 | 1983-08-31 | GebràDer Sulzer Aktiengesellschaft | Clamp for centering the axially slidable shaft of an endoprosthesis inserted into a hollow bone |
FR2549717A1 (en) * | 1983-07-29 | 1985-02-01 | Cuilleron J | Femoral rod with flexible contacts for hip prosthesis |
WO1986006954A1 (en) * | 1985-05-23 | 1986-12-04 | Labor Für Experimentelle Chirurgie Schweizerisches | Self-locking stemmed component for a joint endo-prosthesis |
US4792339A (en) * | 1985-05-23 | 1988-12-20 | Laboratorium Fur Experiementelle Chirurgie, Forschungsinstitut | Self-locking stemmed component for a joint endo-prosthesis |
FR2610823A1 (en) * | 1987-02-12 | 1988-08-19 | Cuilleron J | Improved femoral rod for hip prostheses |
FR2628628A1 (en) * | 1988-03-15 | 1989-09-22 | Omci Sa | Femoral implant for hip replacement - comprises hollow conical shaft with gripping inserts pushed outwardly through peripheral opening by internal conical member |
EP0427902A1 (en) * | 1989-11-16 | 1991-05-22 | SULZER Medizinaltechnik AG | Rectilinear stam for hip joint prosthesis |
CH680110A5 (en) * | 1989-11-16 | 1992-06-30 | Sulzer Ag | |
US5133770A (en) * | 1989-11-16 | 1992-07-28 | Sulzer Brothers Limited | Shaft for prosthesis |
Also Published As
Publication number | Publication date |
---|---|
DE3113898A1 (en) | 1982-10-21 |
IT8212498A0 (en) | 1982-04-06 |
IT1192949B (en) | 1988-05-26 |
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