Classifications

• • 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
  • A61F2/2846—Support means for bone substitute or for bone graft implants, e.g. membranes or plates for covering bone defects
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
  • A61B17/56—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
  • A61B17/58—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
  • A61B17/68—Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
  • A61B17/80—Cortical plates, i.e. bone plates; Instruments for holding or positioning cortical plates, or for compressing bones attached to cortical plates
  • A61B17/8095—Wedge osteotomy devices
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
  • A61B17/14—Surgical saws ; Accessories therefor
  • A61B17/15—Guides therefor
  • A61B17/151—Guides therefor for corrective osteotomy
  • A61B17/152—Guides therefor for corrective osteotomy for removing a wedge-shaped piece of bone
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
  • A61B17/56—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
  • A61B17/58—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
  • A61B17/68—Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
  • A61B17/80—Cortical plates, i.e. bone plates; Instruments for holding or positioning cortical plates, or for compressing bones attached to cortical plates
  • A61B17/8061—Cortical plates, i.e. bone plates; Instruments for holding or positioning cortical plates, or for compressing bones attached to cortical plates specially adapted for particular bones
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
  • A61B2017/00004—(bio)absorbable, (bio)resorbable, resorptive
• • 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
  • A61F2002/30003—Material related properties of the prosthesis or of a coating on the prosthesis
  • A61F2002/3006—Properties of materials and coating materials
  • A61F2002/30062—(bio)absorbable, biodegradable, bioerodable, (bio)resorbable, resorptive
• • 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
  • A61F2002/30772—Apertures or holes, e.g. of circular cross section
  • A61F2002/30784—Plurality of holes

Definitions

• the present invention relates to an implant system for promoting an osteosynthetic process at a gap between two bone fragments on a bone of an endoskeleton, particularly of a human mammal.
• Fractures of bones in the mammalian endoskeleton involve lengthy healing processes.
• the fractures are often stabilized by attaching plates of an implant system to the respective bone, with sections of the bone being fixed relative to one another.
• Such a system is disclosed, for example, in EP 1 440 664 Bl.
• the human wrist is an important building block for coping with many everyday situations with ease. This very important joint is very often affected by injuries.
• the bony basis of the forearm is formed by the radius (spoke) and ulna (ulna). Both are curved.
• a corrective osteotomy is therefore carried out in the case of incorrectly healed radius/ulna fractures, which can lead to the complete elimination of the symptoms.
• a gap can arise during the reconstruction of the radius or ulna due to the correction angle.
• this is nowadays filled with spongiosa, for example from the iliac crest or other donor regions.
• the gap between the two bone fragments can also be left unfilled up to a certain size or filled with a synthetic block.
• the removal from the iliac crest is an additional painful procedure for the patient, which is also associated with risks.
• this filling material must be shaped intraoperatively by sawing and milling. This can only be done with limited accuracy and costs valuable operating time. If the gap between the two bone fragments remains unfilled, this results in a longer healing time, less stability during the healing phase and possibly aesthetic disadvantages.
• the aim is therefore still to supply the gap with an implant that preferably supports healing. It is therefore the object of the present invention to create an implant system that allows a patient-specific bony reconstruction of a bone, in particular of the ulna and radius.
• an implant system having the features of claim 1 .
• an augmentation is provided which can be inserted into the gap between the two bone fragments.
• an osteosynthesis plate is provided, which is set up to be attached to the bone and to the augmentation.
• a connecting device for directly connecting the augmentation and the osteosynthesis plate is also provided.
• the osteosynthesis plate can have at least two plate areas, one of which can be fastened to an associated proximal bone section or distal bone section of the bone in question on both sides of the gap between the two bone fragments, so that with the plate areas fastened in each case the bone sections are held in a defined manner relative to one another.
• the osteosynthesis plate can be attached securely and easily to the relevant bone if the plate areas of the osteosynthesis plate each have at least one fixing element that fixes the respective plate area to the associated bone section of the bone.
• a plurality of fixing elements can also be provided in one or more plate areas.
• the plate areas of the osteosynthesis plate can each be provided with a hole arrangement with at least one hole through which the at least one fixing element reaches in order to be easily connected to the associated bone section.
• the shape of the respective hole arrangement can be designed here, for example, according to load criteria and can thus differ from the one or more other hole arrangements.
• the at least one hole of the respective hole arrangement can pass through the cross section of the osteosynthesis plate, preferably perpendicularly, but other directions are also conceivable.
• the at least one fixing element for fixing the plate areas can advantageously be designed to be resorbable, so that later stressful removal of the same as well as possible complications associated therewith can be omitted.
• the at least one fixing element can be made of a metallic material that has the necessary rigidity for the load-bearing stabilization of the fracture or the gap between two bone fragments.
• connection device can be provided with one or a plurality of holding elements which hold the augmentation on the osteosynthesis plate.
• One or more identical, but also different holding elements can be provided.
• a first holding element can be designed as at least one projection which protrudes from the osteosynthesis plate essentially transversely to the direction of extension of the bone and at least partially encloses the augmentation on its circumference.
• the projections of the first holding element are not limited in number.
• the protrusion of the at least one protrusion essentially transversely to the direction of extension of the bone does not rule out the possibility that the protrusion itself can also have a shape that has curvatures in order to adapt to structures arranged opposite it.
• the first holding element can preferably project with two projections at the height of the augmentation on both sides of the osteosynthesis plate and at least partially encompass the augmentation in the tangential direction. With the two projections, the holding element can hold and guide an augmentation in a suitable manner without having to damage its structure
• the projection(s) of the first holding element can particularly preferably form a form fit with at least one area of that section of the augmentation which they are opposite, such that the augmentation can be arranged without tension on the holding element.
• the end of the at least one projection facing away from the osteosynthesis plate can engage in a respective recess on the augmentation that is assigned to it.
• a plurality of projections each engaging in recesses can also be provided.
• the at least one projection can preferably be provided with at least one undercut on its end facing away from the osteosynthesis plate in such a way that the projection is held particularly well in the respective recess.
• implant system is formed with a second holding element by one or more screws, nails, pins or similar elements or a combination of these, which protrude from the osteosynthesis plate and engage in the augmentation and have good load-bearing properties.
• the second holding element can be designed to be resorbable from a hybrid component, from composites, from a ceramic, from a metal or a polymer.
• the augmentation itself can be resorbable for fracture treatment and should degrade homogeneously for stabilization; moreover, there can be good biocompatibility and healing can be supported functionally. This is also sought for the holding elements and is the case with the above-mentioned materials for the holding elements, in particular also the second holding elements.
• polymers used here can consist of sugar-containing derivatives such as poly[L-lactide] or the like, which are enzymatically degradable, or of polyhydroxybutyric acids (PHB), whereas composites consist of inorganic, organic or mixed components that are biocompatible and can form hydroxyapatite (HA) can convert and can be provided with coatings.
• HA forms a composite of high porosity, good biomechanical properties and high load limit.
• Bioceramics also have good biocompatibility and can, for example, have compositions of HA and alpha- and beta-tricalcium phosphates, which, for example, can have proportions that degrade at different rates.
• Biodegradable metals where the mechanical properties in the foreground can be magnesium (Mg), zinc (Zn) or iron (Fe), for example, without this list being complete.
• a third holding element can be provided, which extends through the augmentation and which has a closed cross section. This enables a more variable definition of the augmentation.
• the third holding element can be designed with an elongate, flexible structure that connects the augmentation to the osteosynthesis plate and engages through two openings in the osteosynthesis plate. This makes the fixation even more flexible and variable, since the structure of the holding element allows a flexible path within the augmentation.
• the third holding element can also be made of an absorbable material, in particular the third holding element can be made of an absorbable metal or a polymer.
• a positioning device with at least one guide means is assigned to it, at the proximal end of which at least one template for introducing the gap in the bone is arranged.
• the gap between the two bone fragments can be pre-planned in a suitable manner and with as little stress as possible, specific to the patient and treatment, and entered into the bone at the desired time.
• the guide means has at least two arms at its distal end, the ends of which form pre-planned reference points that determine the position of the positioning device in relation to the bone, whereby one or more gaps between two bone fragments are produced in a targeted manner to correct fractures can become.
• 1 shows a side view of a first embodiment of the implant system according to the invention with the augmentation;
• Fig. 9 is a cross-sectional view of the embodiment of Fig. 4 along the line
• FIG. 10 shows a perspective view of a positioning device associated with the implant system and arranged on the forearm for introducing a gap between two bone fragments in an ulna and a radius bone.
• FIG. 1 is a side view of a first embodiment of the implant system according to the invention with the augmentation.
• reference numeral 100 designates an implant system for promoting an osteosynthetic process at a gap between two bone fragments 14, e.g., an osteotomy gap 40, on a bone 50 of the endoskeleton of a human mammal.
• An augmentation 10 is inserted with a precise fit into the gap previously planned in the bone between the two bone fragments 40 , and an osteosynthesis plate 20 is attached to the bone 50 and to the augmentation 10 , facing the viewer.
• the osteosynthesis plate 20 has two plate areas 21, 22, one of which is attached to an associated proximal bone section 51 or distal bone section 52 of the bone 50 on either side of the gap between the two Bone fragments 40 are attached, whereby the two bone sections 51, 52 are held in defined alignment with one another.
• One plate area 21 extends with mutually parallel side edges essentially along the shaft of the bone 50 on the proximal bone section 51.
• the other plate area 22 widens in accordance with the two-dimensional expansion of the head of the bone 50 in the distal bone section 52 in the image plane and on the other hand it has an angle with respect to the plane spanned by the plate area 21 of the proximal bone section 51 .
• the two plate areas 21 , 22 of the osteosynthesis plate 20 each have a number of fixing elements 24 which fix the respective plate area 21 , 22 to the associated bone section 51 , 52 of the bone 50 .
• the plate areas 21, 22 of the osteosynthesis plate 20 are each provided with a hole arrangement 26 with a plurality of holes 28 through which the respective fixing element 24 engages.
• the fixing elements 24 are also screws or pins, for example.
• FIGS. 2 and 3 are two side views from different perspectives of a further embodiment of the implant system according to the invention with the augmentation.
• FIGS. 2 and 3 The embodiment according to FIGS. 2 and 3 is identical except for the different retaining element 33 for fixing the augmentation 10 to the osteosynthesis plate 20 .
• 2 shows a side of the bone 50 facing away from the osteosynthesis plate 20, while the representation of FIG. 3 is similar to that of FIG.
• the holding element 33 according to FIGS. 2 and 3 is made of an absorbable polymer with an elongated, flexible structure in the manner of a thread, which connects the augmentation 10 to the osteosynthesis plate 20 and in turn reaches through the two holes L1, L2 of the osteosynthesis plate 20.
• the holding element 33 in the form of a thread also reaches through the porous structure of the augmentation 10 and has a closed longitudinal extent.
• 4 to 8 are side views from different angles of further embodiments of the implant system according to the invention with the augmentation and corresponding holding elements.
• the connecting device 30 is provided with holding elements 31 which hold the augmentation 10 on the osteosynthesis plate 20.
• FIG. 4 to 8 show side views from different angles, while FIG. 9 shows a cross-sectional view along the line IX-IX of FIG.
• the implant system 100 shown in FIG. 4 is identical to that according to FIG. 1 except for the different holding element 31 .
• the first holding element 31 of the connecting device 30 according to FIG. 4 is formed at the height of the augmentation 10 in the form of projections 34a, 34b, which for the observer project transversely to the direction of extension of the bone 50 to the left of the osteosynthesis plate 20 and the augmentation 10 on it Enclose the scope at least in sections.
• FIG. 5 This can be seen in FIG. 5, in which the bone 50 with the osteosynthesis plate 20 and the holding element 31 is rotated counterclockwise by 90° about the longitudinal axis of the bone 50.
• FIG. 6 shows that the holding element 31 with the two projections 34a, 34b at the height of the augmentation 10 projects on both sides of the osteosynthesis plate 20 essentially transversely to the direction of extension of the bone 50 and partially encompasses the augmentation 10 in the circumferential direction, with This representation shows the free ends of the projections 34a, 34b.
• the augmentation 10 is fixed laterally by the projections and axially by the bone regions 51 , 52 .
• the projections 34a, 34b of the first holding element 31 form a form fit with at least one area of that section of the augmentation 10 which they are opposite.
• Bone 50 is rotated a further 90° about the longitudinal axis in FIG. 7, the embodiment shown there differing further from that in FIG a respective recess 12 assigned to these engage in the augmentation 10, only the projection 34a being shown in FIG.
• FIGS. 4 and 5 shows a representation of the implant system shown in FIGS. 4 and 5 with the projection 34b as the retaining element 31, which here engages with its end facing away from the osteosynthesis plate 20 in a recess 12 on the augmentation 10 assigned to it.
• Fig. 9 is a cross-sectional view of the embodiment of Fig. 4 along line IX-IX.
• FIG. 9 is a perspective view of a forearm positioning device associated with the implant system of the present invention for introducing a gap between two bone fragments 40 into an ulna and a radial bone.
• the positioning device 60 for introducing the gap between the two bone fragments 40 into an ulna bone and a radius bone is shown in the state arranged on the bone sections 51, 52, with the positioning device 60 being assigned guide means 62a, 62b , at the proximal ends of which resection templates 64, 66 for introducing osteotomy gaps 40 (not shown here) into the bone 50 are arranged.
• the guide means 62b, 62b each have two arms 65 at their distal ends, which form predetermined reference points 67a-67d, which determine the position of the positioning device 40 in relation to the bone 50, and which are held in place by means of holding means not further identified, for example in the form of K -Wires are held at the distal end of each bone 50 in a definite position.
• the desired osteotomies in the form of the osteotomy gap 40 can be indicated by saw slots 68 for the exact resection for conventional saws or also by several K-wire guides 69. With these, the osteotomy is pre-perforated by several twisted-in K-wires (not shown), then mobilized by small bone chisels (also not shown). Here, not only straight but also curved gaps between two bone fragments 40 can be realized. In addition, there is the advantage that only minimal parts of the bone 50 have to be removed
• Exact positioning of the resection templates 64, 66 in the area of the bone 50 to be provided with the gap between the two bone fragments 40 is achieved without tilting and in a stable, point or line-shaped contact in the respective area, so that such templates 64, 66 can even be used without Support from navigation systems for positioning must be applied safely and clearly. This enables a precise bone resection along the borders of the augmentation 10 and ensures that it fits well.
• a bioactive material e.g.
• Bio-ink to speed up the healing process.

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• Health & Medical Sciences (AREA)
• Orthopedic Medicine & Surgery (AREA)
• Life Sciences & Earth Sciences (AREA)
• Surgery (AREA)
• Public Health (AREA)
• General Health & Medical Sciences (AREA)
• Biomedical Technology (AREA)
• Heart & Thoracic Surgery (AREA)
• Engineering & Computer Science (AREA)
• Veterinary Medicine (AREA)
• Animal Behavior & Ethology (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Medical Informatics (AREA)
• Molecular Biology (AREA)
• Transplantation (AREA)
• Oral & Maxillofacial Surgery (AREA)
• Neurology (AREA)
• Vascular Medicine (AREA)
• Cardiology (AREA)
• Dentistry (AREA)
• Prostheses (AREA)
• Surgical Instruments (AREA)
• Paper (AREA)
• Electrotherapy Devices (AREA)
• External Artificial Organs (AREA)

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• 2020
  • 2020-08-06 DE DE102020209981.2A patent/DE102020209981A1/de active Pending
• 2021
  • 2021-07-17 AU AU2021323330A patent/AU2021323330A1/en active Pending
  • 2021-07-17 EP EP21752499.0A patent/EP4167881A1/de active Pending
  • 2021-07-17 JP JP2023507574A patent/JP2023536332A/ja active Pending
  • 2021-07-17 CN CN202180057756.8A patent/CN116113374A/zh active Pending
  • 2021-07-17 US US18/040,453 patent/US20230320858A1/en active Pending
  • 2021-07-17 WO PCT/EP2021/070064 patent/WO2022028862A1/de unknown
  • 2021-07-17 BR BR112023001273A patent/BR112023001273A2/pt unknown

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