WO2012048689A4 - Knochenverankerungseinrichtung - Google Patents
Knochenverankerungseinrichtung Download PDFInfo
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- WO2012048689A4 WO2012048689A4 PCT/DE2011/050035 DE2011050035W WO2012048689A4 WO 2012048689 A4 WO2012048689 A4 WO 2012048689A4 DE 2011050035 W DE2011050035 W DE 2011050035W WO 2012048689 A4 WO2012048689 A4 WO 2012048689A4
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- bone
- support
- anchoring device
- bone anchoring
- screw
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- 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
- A61B17/84—Fasteners therefor or fasteners being internal fixation devices
- A61B17/86—Pins or screws or threaded wires; nuts therefor
- A61B17/8625—Shanks, i.e. parts contacting bone tissue
- A61B17/863—Shanks, i.e. parts contacting bone tissue with thread interrupted or changing its form along shank, other than constant taper
-
- 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
- A61B17/84—Fasteners therefor or fasteners being internal fixation devices
- A61B17/86—Pins or screws or threaded wires; nuts therefor
- A61B17/8625—Shanks, i.e. parts contacting bone tissue
- A61B17/8635—Tips of screws
-
- 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
- A61B17/84—Fasteners therefor or fasteners being internal fixation devices
- A61B17/86—Pins or screws or threaded wires; nuts therefor
- A61B17/864—Pins or screws or threaded wires; nuts therefor hollow, e.g. with socket or cannulated
-
- 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
- A61B17/84—Fasteners therefor or fasteners being internal fixation devices
- A61B17/86—Pins or screws or threaded wires; nuts therefor
- A61B17/8685—Pins or screws or threaded wires; nuts therefor comprising multiple separate parts
-
- 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
- A61B17/88—Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
- A61B17/885—Tools for expanding or compacting bones or discs or cavities therein
- A61B17/8852—Tools for expanding or compacting bones or discs or cavities therein capable of being assembled or enlarged, or changing shape, inside the bone or disc
- A61B17/8858—Tools for expanding or compacting bones or discs or cavities therein capable of being assembled or enlarged, or changing shape, inside the bone or disc laterally or radially expansible
-
- 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
- A61B17/72—Intramedullary pins, nails or other devices
- A61B17/7233—Intramedullary pins, nails or other devices with special means of locking the nail to the bone
- A61B17/7258—Intramedullary pins, nails or other devices with special means of locking the nail to the bone with laterally expanding parts, e.g. for gripping the bone
- A61B17/7266—Intramedullary pins, nails or other devices with special means of locking the nail to the bone with laterally expanding parts, e.g. for gripping the bone with fingers moving radially outwardly
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00867—Material properties shape memory effect
-
- 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
- A61B17/84—Fasteners therefor or fasteners being internal fixation devices
- A61B17/86—Pins or screws or threaded wires; nuts therefor
- A61B2017/8655—Pins or screws or threaded wires; nuts therefor with special features for locking in the bone
Definitions
- the invention relates to a bone anchoring device which can preferably be implanted for stabilization of the spinal column.
- the anchoring device has a mechanism that clamps the implant between at least two cortical bone sections. The tension takes place so that the distal tip of the bone anchor is pressed by a compressive force against a solid bone layer. This creates a further bearing point, which protects the bone anchor against loosening, especially at bending loads.
- Osteoporosis is characterized by a decrease in apparent bone density, resulting in a reduction in the structural integrity of the bone.
- the clinical challenge in the operative stabilization of such a spinal column is the stable anchoring of implants, which often has insufficient strength due to the reduced bone density. For example, if a pedicle screw is screwed into an osteoporotic vertebra and connected in combination with a dorsal implant system, a bending or lever movement of the distal end of the pedicle screw results due to the bending load.
- pedicle screws can be augmented with bone cement.
- the cement is injected in the liquid state into the cancellous bone of the vertebra. After hardening of the cement block, he offers the pedicle screw, next to the pedicle, another support which increases the stability against screw lever movements (Schultheiss 2002).
- Cement injection involves numerous risks (unwanted cement leakage into the spinal canal, intervertebral disc or the vascular system, necrosis due to high local reaction temperatures, corrosion between implant and X-ray contrast agent admixture). Particularly noteworthy is that the bone cement remains irreversibly in the vertebra and a possibly necessary revision is considerably more difficult.
- cementless bone anchoring devices are known which are designed to increase their diameter after implantation in the bone. Biomechanical studies have shown that they are able to significantly increase the pullout strength, as they have a larger diameter than the pedicle or the insertion opening when clamped (Wan 2010). In some cases, the expandable pedicle screws have a comparable pull-out strength as with cement-augmented pedicle screws (Bostan 2009). In addition, implantable dowels are mentioned (US4011602A 1975; EP0194409B1 1985; US5713904A 1997; US2008221624A1 2005; WO2009120969A2 2008; WO2009155577A2 2008) which have expandable mechanisms.
- a dowel improves the connection, however, only if the wall or the material against which the dowel presses, can apply a corresponding counterforce.
- effective fixation with mechanisms that provide a spreading in the circumferential direction is not possible because the bone density of the surrounding cancellous bone is very low.
- bone anchors for fracture treatment are known, which have been optimized to ensure that axial traction in the bone anchor ensures constant contact of the fracture surfaces (e.g., US 7,601,152 or DE 908906).
- these bone anchors are not suitable for building up an axial compressive force, which is necessary to support against shear movements of the bone anchor within a vertebral body.
- the connection to other components for the rigid fixation of two or more vertebral bodies is not feasible.
- the object of the present invention is therefore to provide an implant which is capable of firmly anchoring in the bone, in particular in the osteoporotic vertebral body.
- the anchoring device should be braced axially between at least two cortical sections in the vortex, so that at least two bearings arise, which offer the anchoring device a higher stability against bending stress.
- the anchorage device in such a way that it is easy implantable and revisable.
- the anchoring device generates a compressive stress between at least two cortical layers in the vortex.
- this can be achieved by the anchoring device extending to the anterior vertebral edge, producing an anterior support surface there by means of a spreading device, and posteriorly the pedicle or the posterior vertebral body wall surrounding the pedicle forms a posterior support surface and both support surfaces are braced against each other by a compressive force become.
- An alternative possibility is to generate the bicortical tension directly on the pedicle by here a distal expansion element is braced against a sleeve.
- the sleeve is characterized in that it applies the counter tension either by a collar, or in the form of a bone thread located in the pedicle.
- the strength of the connection to the bone with the anchoring device, in particular against rotation can be increased by additionally extending elements from the screw shaft into the surrounding cancellous bone.
- An advantage of the present invention is that the implant according to the invention achieves a significant gain in stability compared to other anchoring devices, in particular in the case of osteoporotic bone.
- the additional support and the simultaneous axial clamping reduce the susceptibility of the anchoring device to bending loads. This significantly reduces screw lever movements and thus screw loosening.
- the implant according to the invention can be easily and completely removed from a vertebra.
- Fig. 1 shows the implantable invention for fixation of a vertebra.
- Fig. 2 describes the first embodiment of the invention using the example of a braceable pedicle screw.
- Fig. 3 explains the spreading mechanism.
- Fig. 4 shows a second embodiment possibility and the use of a compression spring for maintaining the axial preload.
- Fig. 5 illustrates a possibility of bicortical support of a pedicle screw on the pedicle.
- Fig. 6 shows a further embodiment of the pedicle screw, wherein the tension of the screw in the vertebral body and in the pedicle is combined.
- Fig. 7 shows the implantation order of the embodiment shown in Fig. 6.
- FIG. 8 shows a modification of the embodiment shown in FIG. 6 in that the pedicle screw can adapt its length.
- Fig. 9 shows another modification of the previous embodiment.
- Fig. 10 illustrates the fifth embodiment of the clampable pedicle screw.
- Fig. 11 shows a modification of the embodiment shown in Fig. 10.
- FIG. 12 shows a pedicle screw with spreading elements that can be extended distally from the screw shaft.
- Fig. 13 shows an alternative embodiment in which the spreading can be moved without thread.
- the implant (2) according to the invention can be implanted in a vertebra (1) (FIG. 1).
- the pedicle screw (1) consists of a distal (10), a middle (20) and a proximal shaft component (30), wherein on the proximal component at least one head part (40) is attached, which serves to the screw with a dorsal component connect.
- This dorsal component serves to connect to a connecting element, e.g. a rod, which is typically connected to other bone anchors and thus further vertebral bodies.
- the screw head (40) is varied in the following embodiments to simultaneously show a polyaxial and monoaxial connection variant.
- the pedicle screw may include a throughbore (50) for application over a guidewire and / or for receiving components of a spreading mechanism.
- the main components may be designed so that they can be combined with each other and / or interchangeable.
- at least one of the components may include an elastically deformable region (e.g., 3101) or a resilient element (419, 6160). This component acts as a spring that can store a preload force and compensate for any changes in the depth of engagement of the pedicle screw.
- the pedicle screw is clamped between the anterior (101) and posterior vertebral body edges (102).
- the pedicle screw consists of a threaded screw shank (320) which merges with the proximal screw shank (330), a screw head (340) and a central throughbore (350).
- the pedicle screw (3) is characterized in that it has a distal support device (310) (Fig. 2).
- the distal support device (310) includes spreading elements (3101).
- the spreading elements can be adjusted by suitable pretreatment so that they have the tendency to bend or curve in the circumferential direction, which is initially prevented by a closure cap (311, 312, 313) for implantation.
- the spreading elements (3101) may have at their ends a contour (3102) e.g.
- the cap (312) can be provided on the circumference with additional profile attachments (3112), which have the task of securing the cap (312) from self-rotation when the cap (312) is axially biased or removed in the context of a revision.
- the head of the closure cap (3113) may be supported on the anterior vertebral edge (101) in addition to the expansion elements (3101).
- the surface or the entire cap head (311, 312, 313) can be designed so that it has an increased friction and at the same time allows a large contact surface.
- the increased friction or ingrowth of the closure cap head (313) and / or the spreading elements (3101) can be achieved, for example, by a porous coating, roughening or a coating with osteoconductive or osteoinductive materials such as (tri) calcium phosphate, hydroxilapatite, BMP or RGD become.
- a connecting rod (352) is fixed in the cap (e.g., 313).
- the connecting rod is mounted in a connecting sleeve (351) and freely accessible at the proximal outlet of the pedicle screw.
- the connecting sleeve (351) is firmly connected to the distal support device (310) and rotatably mounted in the through hole (350) of the pedicle screw (3).
- the pedicle screw (31) is first implanted in the vertebra (FIG. 3). Subsequently, (32) the connecting rod (352) is inserted into the connecting sleeve (351) and connected to the cap (311) e.g. Threaded (3115). Now, the connecting rod is pushed in the anterior direction, so that the cap of the spreading elements (3101) dissolves and releases them. The spreading elements (3101) unfold (33) due to their residual stress or due to a deeper insertion of the pedicle screw (3) in the anterior direction. If a tensile force is applied to the connecting rod (352), the cap (3115) connected thereto can also be used for further spreading of the spreading elements (3101) (illustration 34 in FIG. 3).
- the distal support device (310) may initially be inserted and opened without the screw shaft (320, 330, 340). This is followed by screwing in the proximal screw shaft (330) via the connecting sleeve (351). Screwing in the screw shaft (330) can thus be used simultaneously to adjust the preload of the pedicle screw (3).
- the pedicle screw (4) consists of a distal support device (410) with spreading elements (4101), a central shaft region (420), a proximal shaft region (430), a screw head (440) and a through-bore (450) (FIG 4).
- this embodiment is similar to the previously described pedicle screw (3).
- the central screw shank (420) does not require a thread because the bone anchoring element is bi-tensioned (101, 102), but may include surface modification (roughening, coating) for osteoinduction or augmentation of osteointegration.
- the middle segment (420) may also be reduced in diameter to provide little dynamics or flexibility of the bone anchoring element.
- a distal support device (410) may also be provided via a spring located on the shaft (420), e.g. a compression spring are biased (419).
- a dedicated anterior support (compare 310, 410) is dispensed with, since the bicortical support is generated on the inner (102) and outer pedicle (103).
- This pedicle screw essentially has a central (520) and a proximal (530) shaft region and a screw head (540) (FIG. 5).
- the proximal screw shaft (530) has a surface suitable for anchoring in the pedicle, e.g. a thread.
- the central screw shaft (520) is equipped with spreading elements (521) which are connected in the distal direction with a threaded sleeve (522).
- the proximal screw shaft may have a collar (531) remote from it, which serves to inter alia. to define the maximum screw-in depth.
- the collar (531) may on the one hand be made of a rigid material (for example steel, titanium or PEEK), but in order to maintain a prestress, it is advisable to equip it with a certain elasticity in the longitudinal direction. This can be achieved, for example, by a compression spring, an elastic material (e.g., PCU, silicone), or by slots or plate-spring layering of corresponding discs.
- an anatomical configuration of the collar (531) adapted to the pit between the transverse process and the facet joint, can bring about an improvement in the supporting action of this bearing.
- the pedicle screw (5) is first screwed (51) into the pedicle up to the proximal shaft collar (531).
- the spreading of the spreading elements (521) can, depending on the embodiment, e.g. done by a rotation of the threaded rod.
- the threaded sleeve (522) is pulled in the direction of the screw head and the spreading elements are moved to the abutment against the posterior vertebral edge (102) (52).
- Decisive here is that the spreading of the screw as in the other variants produce a bias in the screw longitudinal direction to the surrounding bone, and the improved anchoring is not only caused by a radial expansion.
- the support on the pedicle is achieved by a distal extension (510) of the pedicle screw shaft that can be connected to or connected to the screw shaft.
- the support in the region of the vertebra (1) or on the anterior vertebral edge (101) is also supported by conditioning the extension (510) on the ventral cortical vertebral wall and the buildup of a compressive force in the screw shaft to its tension.
- the support device (510) can be connected to the threaded rod (551) or to the threaded sleeve (522), or introduced into the pedicle prior to implantation of the pedicle screw, in which case the threaded rod (551), the threaded sleeve (522) or the screw shaft (530) serves as a guide, which allows the transmission of bending moments and / or axial forces on the supporting device (510).
- a sub-variant of this fourth embodiment variant has a second threaded sleeve at the distal end of the screw.
- the second threaded sleeve presses on the support device (510) and biases it axially, while at the same time placing the expansion elements (521) and bracing them against the dorsal cortex (102).
- the generation of the axial compressive stress in this variant or sub-variant according to the invention is not produced by the screwing depth of the pedicle screw, but by a separate mechanism (for example by an internal threaded spindle).
- the pedicle screw (6) comprises a distal (610), middle (620) and proximal (630) shaft region, and a screw head (640) located on the proximal screw shaft (630). Furthermore, the pedicle screw (6) has a central through-hole (650) (FIG. 6).
- the main feature of this pedicle screw is that the design variants (1 or 2) and (3) are combined herewith in order to benefit from the advantages of the aforementioned embodiments.
- the distal support device (610) has at least two expansion elements (6110), a bearing (6111), guide grooves (6120) and at least one threaded sleeve (6150).
- the guide grooves (6120) have the task of providing a rotation-stable but translatable connection with the central screw component (620), wherein in the guide grooves (6120) distal guide rails (6210) fulfill this function.
- the middle screw component (620) has further guide rails (6230) at the proximal end, which are connected in a rotationally secure and translationally displaceable manner with the proximal screw component (630). There, the guide rails (6230) are mounted in proximal guide grooves (6320).
- the proximal screw component (630) has expansion elements (6310), a threaded sleeve (6350) and a proximal collar (631) similar to the distal support device (610).
- In the central through-hole (650) is a connecting rod (651).
- the screw head (640) may be fixedly connected to either the connecting rod (651) or the proximal collar (631).
- the connecting rod (651) preferably has a bearing at the distal end (6511) and in the central region (6520).
- the connecting rod (651) preferably has two threaded portions (distally 6510 and proximal 6530) disposed in opposite directions such that upon twisting of the connecting rod (651), the distal threaded sleeve (6150) extends further distally and the proximal threaded sleeve (6350) continues proximally be moved.
- the distal bearing (6511 with 6111) and the middle bearing (6520 with 6250) have the task that the central screw component (620) remains in the same position when the spreading elements are clamped at the distal or proximal end simultaneously and that the length of the bone anchor (6) remains constant.
- the pedicle screw (6) is first screwed into the vertebra (FIG. 7). First, the correct pedicle screw length must be determined so that the expansion elements (6110 and 6310) reach their support points in the vertebra. Subsequently, the connecting rod (651) is rotated so that the distal and proximal spreading members (6110 and 6310) are erected (62). At the same time remove the threaded sleeves (6150 and 6350) from the middle screw component (620).
- the spreading elements are positioned and moved apart in the screw longitudinal direction until an optimal tension of the pedicle screw (6) is achieved in the vertebral body.
- Fig. 8 a modification of this embodiment is shown, with which it is possible to automatically adjust the pedicle screw length L of the embodiment (6a) between the anterior (101) and posterior vertebral body edge (102).
- the distal supporting device (610) is connected to the connecting rod (651) via an elastic element, for example a compression spring (6160).
- the connecting rod (651) is free to move along the pedicle screw axis for implantation.
- a rotation of the connecting rod (651) distracts the threaded sleeves (6150 and 6350).
- the distal tip (6111) comes into contact with the anterior vertebral body edge (101) or reaches the maximum adjustment range, the spreaders (6110 and 6310) are placed and the pedicle screw (6a) can axially clamp.
- a simplified distal support (6110) is presented which, by building up a compressive force, spreads and supports directly against the anterior vertebral body edge (101) (FIG. 9).
- This embodiment variant of the support can be implemented distally, proximally or on both regions of the screw shaft or combined with another axial expansion mechanism as described above.
- parts of the distal (710) (FIG. 11), middle (720) (FIG. 10) or proximal (730) shaft region of the pedicle screw can be designed such that they have one or more openings ( 721) opening in the through hole (750) (Fig. 10).
- a rod (751) In the through hole (750) of the pedicle screw (7) is a rod (751), preferably with a guide sleeve (752) attached thereto.
- On or in this guide sleeve are fixed one or more spreading elements (for example in the form of wires), which altogether function as a supporting element (753).
- the spreading elements or wire ends can be rounded, bent or formed blunt with the aid of platelets (754).
- the spreading members / wires (753) may exit the shaft portion either through the central throughbore (750) or through the openings (721).
- the pedicle screw (7) is screwed into the vertebra (71, 73).
- the rod (751) is moved in the distal direction (72, 74), which displaces the support element (s) (753) outwardly through the openings (721) or throughbore (750).
- the wires (753) can be pushed out of the screw inside until they find a cortical vortex edge hold.
- any or all of the wires may be biased to spread on application to the screw shaft in the radial direction, thereby imparting increased resistance to torsion to the screw shaft (730).
- the distal support device is produced from a sleeve which has one or more expansion elements (753).
- the spreading elements are thereby reshaped or pretreated in such a way that they endeavor to expand in the radial direction as soon as they leave the passage openings (721) of the pedicle screw tip (710) (FIG. 12).
- Suitable materials include nitinol, other highly elastic materials or shape memory alloys.
- the pedicle screw (75) is constructed so that the spreading elements are attached to a guide sleeve (752).
- the guide sleeve (752) is guided in the central through hole, has an internal thread and is mounted on a threaded rod (751).
- the expansion elements (753) and the associated passage openings (721) are arranged so that they protect the guide sleeve (752) against rotation.
- the threaded rod (7511) can be rotated, wherein the guide sleeve (752) then moves along the threaded rod (751), which in turn has the expansion or retraction of the expansion elements (753) result.
- an internal threaded rod (751) is dispensed with (FIG. 13).
- the guide sleeve (752), together with the expansion elements (753), can be mounted on an instrument and inserted through the central throughbore (750).
- a fuse element such as e.g. a clamping ring (7521) fixes the position of the guide sleeve (752) within the throughbore (750).
- the clamping ring may be a locking mechanism, an elastic ring which is thicker by axial clamping and thus against the wall (750) is supported or a lock, for example. be used based on a spring washer or wedge-shaped clamping elements.
- the main advantage of this embodiment (76) is that the pedicle screw consists of a continuously cannulated body and the pedicle screw can be minimally invasively implanted over a guide wire.
Abstract
Description
Claims (15)
- Eine Knochenverankerungseinrichtung bestehend aus mindestens einer Schaftkomponente (10, 20, 30) und einem Kopfteil (40), dadurch gekennzeichnet, dass an mindestens einer der Schaftkomponenten ein Abstützelement angebracht ist, welches eine Abstützung der Knochenverankerungseinrichtung primär in deren Längsrichtung erlaubt.
- Eine Knochenverankerungseinrichtung bestehend aus einer proximalen Schaftkomponente (30, 320, 330) mit einem Knochengewinde sowie einem Kopf (340) zur Anbindung an ein Implantatsystem zur Stabilisierung der Wirbelsäule, dadurch gekennzeichnet dass sich im distalen Bereich des Schafts eine Abstützvorrichtung (310, 510, 610, 753) befindet, die dazu geeignet ist, sich an der anterioren Wand (101) eines Wirbelkörpers von innen heraus abzustützen, die über mindestens ein Verbindungselement (351, 352, 551, 752) mit dem Schraubenschaft (30) verbunden ist und die relativ zu diesem in Längsrichtung einstellbar ist.
- Eine Knochenverankerungseinrichtung bestehend aus einer Schaftkomponente (30, 630, 730) mit einem Knochengewinde und einem Kopf (640, 740) zur Anbindung an ein Implantatsystem zur Stabilisierung der Wirbelsäule, dadurch gekennzeichnet dass sich innerhalb des Schafts eine in Längsrichtung der Knochenverankerungseinrichtung wirkende Abstützvorrichtung (610, 6110, 753) befindet, die mittels mindestens einem Stellelement (551, 651, 751) aus Aussparungen innerhalb des Schaftbereichs herausfahrbar ist.
- Eine Knochenverankerungseinrichtung nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet dass die Abstützvorrichtung im Wesentlichen aus Armen (3101, 753) besteht, die mit einem Verstellelement (351, 651, 751) verbunden sind wodurch die Ausfahrlänge der Arme einstellbar ist.
- Eine Knochenverankerungseinrichtung nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet dass die Arme (3101, 753) der Abstützvorrichtung an deren distalen Enden abgerundet, abgebogen oder mit Tellern versehen sind, die dazu geeignet sind den Widerstand gegen eine Penetration oder Fraktur des angrenzenden Knochens zu erhöhen.
- Eine Knochenverankerungseinrichtung nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet dass die Arme (3101, 753) der Abstützvorrichtung an deren distalen Enden durch ein Verschlusselement (311, 312, 313, 411) zusammengehalten werden und das Verschlusselement zur Aufhebung des Zusammenhalts in der Schraubenlängsachse verschoben werden kann.
- Eine Knochenverankerungseinrichtung mit einer Abstützvorrichtung bestehend aus federelastischen Armen (3101, 753) und einem Verschlusselement (311, 312, 313, 411) zum Zusammenhalt der Arme nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet dass das Verschlusselement am Umfang eine Oberflächenkontur aufweist, die dazu geeignet ist die Arme nach Aufhebung des Zusammenhalts weiter im Durchmesser aufzuspreizen und dass das Verschlusselement (311, 312, 313, 411) in Längsrichtung der Schraubenachse verstellbar gelagert ist.
- Eine Knochenverankerungseinrichtung bestehend aus einer proximalen Schaftkomponente (530, 630) mit einem Knochengewinde und einem Kopf (540, 640) zur Anbindung an ein Implantatsystem zur Stabilisierung der Wirbelsäule, dadurch gekennzeichnet dass sich im distalen Bereich des Schafts eine Abstützvorrichtung (520, 521) zur Abstützung gegen kortikalen Knochen befindet, und sich diese Abstützvorrichtung sowohl im Durchmesser aufweiten als auch in Längsrichtung zur Schraubenachse verschieben lässt.
- Eine Knochenverankerungseinrichtung bestehend aus einer proximalen Schaftkomponente (630) mit einem Knochengewinde und einem Kopf (640) zur Anbindung an ein Implantatsystem zur Stabilisierung der Wirbelsäule, dadurch gekennzeichnet dass sich im Schaftbereich (620) zwei Abstützvorrichtungen (6110, 6310) zur Abstützung gegen kortikalen Knochen befinden die sich über ein Stellelement (551, 651) sowohl im Durchmesser aufweiten als auch in Längsrichtung zur Schraubenachse zum Aufbau einer Druckkraft in der Knochenverankerungseinrichtung verschieben lassen.
- Eine Knochenverankerungseinrichtung mit mindestens einem Abstützelement gemäß einem der vorherigen Ansprüche, dadurch gekennzeichnet dass die im Wesentlichen in Schraubenlängsachse verlaufenden Arme des Abstützelements (521, 6110, 6310) mit vorgeprägten Knicken oder Ausnehmungen versehen sind, und die Arme des Abstützelements mit einem Verbindungselement (522, 6150, 6350) verbunden sind oder eine Einheit bilden, welches andererseits mit einem Verstellelement (551, 651) verbunden ist.
- Eine Knochenverankerungseinrichtung nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet dass mindestens ein Abstützelement (410, 610, 6110, 6111) mit einem in Längsrichtung des Knochenankers wirkenden federelastischen Element (419, 6160) verbunden ist um sich gegen eine anteriore und / oder dorsale kortikale Wand eines Wirbelkörpers abzustützen und dagegen eine Druckkraft aufzubauen.
- Eine Knochenverankerungseinrichtung nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet dass die Spreizelemente (610, 6110, 6111, 753) mit einem in Längsrichtung des Knochenankers wirkenden Verstellelement (651, 751) verbunden sind und das Verstellelement als Gewindespindel mit einem oder zwei gegenläufigen Gewinden ausgebildet ist.
- Eine Knochenverankerungseinrichtung nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet dass die Spreizelemente (610, 6110, 6111, 753) mit einem in Längsrichtung des Knochenankers wirkenden Verstellelement (651, 751) verbunden sind, das Verstellelement als Zug- oder Druckstab ausgebildet ist und mit einem Klemmmechanismus versehen ist, welcher dazu geeignet ist den Zug-/Druckstab in jeder Position gegen die Wandung einer Bohrung (50, 750) zu verspannen und damit in seiner Längsposition zu arretieren.
- Eine Knochenverankerungseinrichtung nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet dass die Spreizelemente (610, 6110, 6111, 753) aus einem hochelastischen oder plastisch verformbaren Material hergestellt sind, insbesondere aus Nitinol, einer Kobalt-Chrom-Legierung, einer Titanlegierung, aus Reintitan oder aus einem hochfesten Kunststoff wie PEEK oder PEKK.
- Methode zur Implantation einer Knochenverankerungseinrichtung mit einer in Längsrichtung wirkenden Abstützeinrichtung und Ausbringung der Abstützeinrichtung, bestehend aus den Schritten:Präparation der Implantationsstelle;Eröffnen des Knochens mit einem scharfkantigen Instrument;Implantation der Knochenverankerungseinrichtung mit Hilfe eines Implantations-Instruments;Ausbringung der Abstützeinrichtung mit einem Instrument bis die Abstützeinrichtung am kortikalen Knochen anliegt.
Priority Applications (1)
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DE112011104236T DE112011104236A5 (de) | 2010-09-22 | 2011-09-21 | Knochenverankerungseinrichtung |
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DE201010041226 DE102010041226A1 (de) | 2010-09-22 | 2010-09-22 | Knochenverankerungseinrichtung |
DE102010041226.0 | 2010-09-22 |
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WO2012048689A2 WO2012048689A2 (de) | 2012-04-19 |
WO2012048689A3 WO2012048689A3 (de) | 2012-07-26 |
WO2012048689A4 true WO2012048689A4 (de) | 2012-09-27 |
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PCT/DE2011/050035 WO2012048689A2 (de) | 2010-09-22 | 2011-09-21 | Knochenverankerungseinrichtung |
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WO (1) | WO2012048689A2 (de) |
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EP3612113B1 (de) * | 2017-04-21 | 2023-06-14 | Stryker Corporation | Stabilisierungssystem und implantat zur verhinderung der relativen bewegung zwischen gewebeschnitten |
CN112402001B (zh) * | 2020-09-11 | 2022-03-08 | 南昌大学第二附属医院 | 骨科脊柱手术的椎体万向复位装置 |
DE102020134637A1 (de) * | 2020-12-22 | 2022-06-23 | Asklepios Orthopädische Klinik Hohwald | Modulare chirurgische Knochenexzenterschraube |
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DE908906C (de) | 1950-06-02 | 1954-04-12 | Dr Med H C Ernst Pohl | Federnde Knochenschraube, besonders fuer Schraeg- und Laengsbrueche |
US4011602A (en) | 1975-10-06 | 1977-03-15 | Battelle Memorial Institute | Porous expandable device for attachment to bone tissue |
CN1006954B (zh) | 1985-03-11 | 1990-02-28 | 阿图尔·费希尔 | 用于骨接合术的紧固元件 |
DK0567423T3 (da) | 1992-04-24 | 1997-03-10 | Bilbao Ortiz De Zarate Jos Ram | Transpediculære vertebrale fastgørelsessystemer og indretning til praktisering deraf |
US5713904A (en) | 1997-02-12 | 1998-02-03 | Third Millennium Engineering, Llc | Selectively expandable sacral fixation screw-sleeve device |
CA2452508C (en) * | 1998-10-26 | 2010-09-14 | Expanding Orthopedics Inc. | Expandable orthopedic device |
DE19922440A1 (de) | 1999-05-06 | 2000-11-09 | Schaefer Micomed Gmbh | Pedikelschraube |
DE19949285C2 (de) | 1999-10-12 | 2002-08-14 | Impag Gmbh Medizintechnik | Knochenschraube |
US6668688B2 (en) * | 2001-06-28 | 2003-12-30 | Mayo Foundation | Expandable screw apparatus and method thereof |
US20080221624A1 (en) | 2005-10-17 | 2008-09-11 | Gooch Hubert L | Systems and Methods for the Medical Treatment of Structural Tissue |
US7789901B2 (en) | 2007-10-11 | 2010-09-07 | Zimmer Gmbh | Bone anchor system |
ES2607605T3 (es) * | 2007-12-28 | 2017-04-03 | Biedermann Technologies Gmbh & Co. Kg | Implante para estabilizar vértebras o huesos |
EP2306913A4 (de) | 2008-03-28 | 2014-06-04 | Warsaw Orthopedic Inc | Knochenanker für orthopädische anwendungen |
KR20110033199A (ko) | 2008-06-19 | 2011-03-30 | 신세스 게엠바하 | 뼈 스크류 퍼처스 증강 임플란트, 시스템 및 기술 |
WO2010105196A1 (en) * | 2009-03-13 | 2010-09-16 | University Of Toledo | Removable anchoring pedicle screw |
US9215470B2 (en) | 2010-07-09 | 2015-12-15 | Qualcomm Incorporated | Signaling selected directional transform for video coding |
-
2010
- 2010-09-22 DE DE201010041226 patent/DE102010041226A1/de not_active Withdrawn
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2011
- 2011-09-21 DE DE112011104236T patent/DE112011104236A5/de not_active Withdrawn
- 2011-09-21 WO PCT/DE2011/050035 patent/WO2012048689A2/de active Application Filing
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DE102010041226A1 (de) | 2012-03-22 |
DE112011104236A5 (de) | 2013-11-07 |
WO2012048689A3 (de) | 2012-07-26 |
WO2012048689A2 (de) | 2012-04-19 |
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