US20020013553A1 - Apparatus for the application of bone cement and a cannula for such an apparatus - Google Patents
Apparatus for the application of bone cement and a cannula for such an apparatus Download PDFInfo
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- US20020013553A1 US20020013553A1 US09/865,109 US86510901A US2002013553A1 US 20020013553 A1 US20020013553 A1 US 20020013553A1 US 86510901 A US86510901 A US 86510901A US 2002013553 A1 US2002013553 A1 US 2002013553A1
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- United States
- Prior art keywords
- cannula
- accordance
- piston
- cylinder
- bone cement
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C17/00—Hand tools or apparatus using hand held tools, for applying liquids or other fluent materials to, for spreading applied liquids or other fluent materials on, or for partially removing applied liquids or other fluent materials from, surfaces
- B05C17/005—Hand tools or apparatus using hand held tools, for applying liquids or other fluent materials to, for spreading applied liquids or other fluent materials on, or for partially removing applied liquids or other fluent materials from, surfaces for discharging material from a reservoir or container located in or on the hand tool through an outlet orifice by pressure without using surface contacting members like pads or brushes
- B05C17/01—Hand tools or apparatus using hand held tools, for applying liquids or other fluent materials to, for spreading applied liquids or other fluent materials on, or for partially removing applied liquids or other fluent materials from, surfaces for discharging material from a reservoir or container located in or on the hand tool through an outlet orifice by pressure without using surface contacting members like pads or brushes with manually mechanically or electrically actuated piston or the like
- B05C17/0116—Hand tools or apparatus using hand held tools, for applying liquids or other fluent materials to, for spreading applied liquids or other fluent materials on, or for partially removing applied liquids or other fluent materials from, surfaces for discharging material from a reservoir or container located in or on the hand tool through an outlet orifice by pressure without using surface contacting members like pads or brushes with manually mechanically or electrically actuated piston or the like characterised by the piston driving means
- B05C17/0133—Nut and bolt advancing mechanism, e.g. threaded piston rods
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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
- A61B17/88—Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
- A61B17/8802—Equipment for handling bone cement or other fluid fillers
- A61B17/8805—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it
- A61B17/8816—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it characterised by the conduit, e.g. tube, along which fluid flows into the body or by conduit connections
-
- 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
- A61B17/8802—Equipment for handling bone cement or other fluid fillers
- A61B17/8805—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it
- A61B17/8819—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it characterised by the introducer proximal part, e.g. cannula handle, or by parts which are inserted inside each other, e.g. stylet and cannula
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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
- A61B17/88—Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
- A61B17/8802—Equipment for handling bone cement or other fluid fillers
- A61B17/8805—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it
- A61B17/8822—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it characterised by means facilitating expulsion of fluid from the introducer, e.g. a screw pump plunger, hydraulic force transmissions, application of vibrations or a vacuum
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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
- A61F2/46—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
- A61F2/4603—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof
Definitions
- the present invention relates to an apparatus for the application of bone cement having a housing which comprises a cylinder for the reception of the bone cement and having a piston arranged longitudinally displaceably in the cylinder by which the bone cement can be pressed out of an exit aperture formed in the cylinder, with the piston for the application of the bone cement under high pressure being longitudinally displaceable by a screw movement in the cylinder.
- a cannula for an apparatus for the application of bone cement having an aperture formed at the distal end and a coupling section provided at the proximal end for coupling to the application apparatus is further described.
- a plurality of demands must be considered during application.
- the filling of the application apparatus and the application into the affected bone structures must take place very rapidly, within a few minutes, since the bone cements usually used begin to harden 6 to 7 minutes after mixing.
- the bone cement must be applied at a very high pressure, since otherwise sufficient penetration of the bone structures is not ensured.
- the application of the bone cement must be easily controllable, since a misdirecting of the bone cement can lead to irreversible damage, for example to nerves, particularly during application in the region of the spinal column.
- a cannula in accordance with the invention is characterized in that the distal end of the cannula is formed asymmetrically with a tip disposed to the side of the central axis and in that laterally outwardly projecting handling elements are provided at the proximal end of the cannula with which the cannula can be both turned around its longitudinal axis and displaced along its longitudinal axis.
- proximal is used in the meaning of “disposed toward the body of the physician”.
- distal is used accordingly to mean “disposed remote from the body of the physician”.
- the switchability of the application apparatus in accordance with the invention means that it is possible, for example, for the filling of the cylinder to take place in a very short time by a loading movement of the piston, i.e. by a direct displacement of the piston in the longitudinal direction.
- the liquid cement present in the cylinder can, vice versa, subsequently be applied in a short time by a direct displacement of the piston for so long until the counter pressure which is created becomes so large that it can no longer be overcome by the direct advance movement.
- the application apparatus is switched to a mode “displacement of the piston by screw movement”, since a substantially greater pressure can be exerted on the piston, and thus on the bone cement to be applied by the screw movement, than with a direct advance movement.
- a further advantage of the application apparatus formed in accordance with the invention lies in the fact that the high pressure built up during the application with a screw movement can be built up very fast, i.e. within fractions of a second. This is required, for example, when a misdirecting of the bone cement is recognized during the observation, for example at a fluoroscope, of the bone cement exiting the cannula.
- a simple switching of the apparatus to the direct longitudinal displaceability of the piston allows the piston to be pushed back due to the high pressure and thus the pressure to be automatically reduced. In this way, the misdirected exit of the bone cement from the distal end of the cannula is stopped directly.
- the piston comprises an engaging section with a screw thread which engages into a cooperating toothed arrangement provided at the housing so that the longitudinal displacement of the piston takes place when the engaging section is turned.
- the cooperating toothed arrangement can in particular be formed as a rack.
- the screw thread and the cooperating toothed arrangement can be uncoupled, with the cooperating toothed arrangement advantageously being able to be moved substantially perpendicular to the direction of displacement of the piston between a locking position and releasing position for the uncoupling.
- a simple and fast switch from the operating state “displacement by screw movement” into the operating state “direct displacement in the longitudinal direction” and back is made possible by this design, by, for example, the cooperating toothed arrangement being displaced into the release position via an actuating unit attached to the housing.
- the cooperating toothed arrangement is advantageously pressed against the screw thread under bias. It is ensured in this way that the built-up pressure is automatically ensured for so long until the cooperating toothed arrangement is moved against the bias.
- This bias can be effected for example by a loading of a spring.
- the cooperating toothed arrangement grips around the screw thread regionally, in particular free of undercutting.
- An enlarged contact surface between the teeth of the cooperating toothed arrangement contacting one another under high pressure and the thread section of the screw thread is achieved by a regional gripping around of the screw thread so that the stability of the apparatus is increased.
- the gripping around free of undercutting ensures that a simple uncoupling of the screw thread and the cooperating toothed arrangement is still possible, for example by a simple lateral displacement of the cooperating toothed arrangement.
- the piston is preferably substantially freely longitudinally displaceable in the cylinder in the uncoupled state.
- the free displaceability of the piston is essentially only impaired by a seal which is usually provided for sealing between the piston circumference and the inner wall of the cylinder.
- the tooth flanks of the cooperating toothed arrangement and/or the flanks of the thread section of the screw thread which abut one another during the application of the bone cement under pressure form an angle of less than or equal to 90° with the longitudinal axis of the engaging section extending parallel to the direction of displacement. It is ensured by his special formation of the flanks that no overlatching of individual teeth occurs—such as can be the case with normal, chamfered flanks where the angle between the longitudinal axis of the engaging section is greater than 90°—even when very high pressures are used.
- the cooperating toothed arrangement can be displaced by a displacement movement perpendicular to the direction of movement of the engaging section for the uncoupling from the screw thread. If the angles are less than 90°, uncoupling is possible by a corresponding displacement of the cooperating toothed arrangement obliquely to the longitudinal axis of the engaging section.
- the piston and the engaging section are preferably formed in one piece. With a one-piece formation, it must be ensured that the piston is rotatable in the cylinder in order to allow the screwing of the engaging section in this manner. In this embodiment, the longitudinal displacement of the piston is thus directly achieved by screwing in the piston.
- the piston it is also possible for the piston to be formed in two parts so that the engaging section forms a separate part. In this case, both parts are connected to one another, in particular in a manner rotatable against one another. In this embodiment, it is possible for only the engaging section to be rotated in the screw movement, while the piston is forwardly displaced inside the cylinder without rotation by the forward-screwing engaging section.
- the cross-section areas of the piston and the cylinder are complementary to one another, but can be of any shape in principle; for example, they can have an oval or polygonal shape, with the single-piece design of the piston and the engaging section, the cylinder is usually formed as a circular cylinder in order to allow a rotation of the piston in the cylinder together with the engaging section in this manner.
- a cannula is fastenable to the exit aperture of the cylinder.
- This cannula is preferably releasably fastened since, in this way, the cannula can be introduced and positioned in the patient in a first process step without an application apparatus, while the application apparatus can be filled with the liquid bone cement in a second process step only after the successful positioning, for example via a loading cannula likewise attachable to the exit aperture.
- the application apparatus can subsequently be fastened to the already inserted injection cannula and the bone cement applied in the previously described manner.
- the cannula in accordance with the invention has the advantage that as a result of its asymmetrical tip and also the laterally outwardly projecting handling elements, an exact positioning can already be made during the introduction of the cannula.
- Conventional cannulae have a symmetrical tip and cannot be altered with respect to their direction of introduction during introduction.
- the asymmetrical tip can be positioned by a rotation of the partly introduced cannula via the laterally outwardly projecting handling elements such that a movement of the cannula in the desired direction is achieved during the further introduction.
- the cannula will always deviate slightly in the lateral direction to which the tip is just disposed due to the preceding asymmetrical tip.
- the cannula of the invention allows turning or shearing off of the bone cement still hardening inside the cannula from the bone cement applied into the bone structure by turning the cannula still located in the body around its longitudinal access via the handling elements after the hardening of the applied bone cement. It is thereby ensured that the bone cement located inside the cannula remains in it when it is pulled out and is reliably removed from the tissue together with it.
- the edge of the cannula forming the border of the aperture is preferably ground as a cutting edge. A reliable shearing off of the material disposed inside the cannula is thereby also ensured with a completely hardened bone cement.
- the penetration surface of the aperture extends obliquely to the longitudinal axis of the cannula.
- the direction of movement of the bone cement exiting from the aperture in the cannula tip can be controlled in this way.
- the aperture can be positioned by rotating the cannula via the handling elements such that the exiting material flows in the desired direction.
- cannulae having a central aperture such as are known from the prior art, the bone cement, however, always exists forwardly in a longitudinal direction so that the direction of exit cannot be altered by rotating the cannula.
- FIG. 1 a partly cut-open cross-section of an application apparatus formed in accordance with the invention
- FIG. 2 a detailed view of an apparatus of FIG. 1;
- FIG. 3 a partly cut-open cross-section of the apparatus of FIG. 1;
- FIG. 4 a cannula formed in accordance with the invention
- FIG. 5 a detailed view of the cannula of FIG. 4;
- FIG. 6 a further embodiment of a cannula formed in accordance with the invention.
- FIG. 7 a detailed view of the cannula of FIG. 6.
- FIG. 1 shows a pistol-like application apparatus 1 having a housing 2 whose central region is formed as a cylinder 3 for the reception of bone cement at its inside 4 .
- a piston 5 is displaceably supported in the direction of its longitudinal axis 6 inside the cylinder 3 , with the piston 5 being sealed with respect to the inner wall of the cylinder 3 by a sealing means 7 .
- An exit aperture 8 is formed at the distal end of the cylinder 3 and coupling element 9 , formed for example as a large Luer lock connection, is provided thereat for the coupling of a cannula.
- the piston 5 is formed in one piece with an elongated shaft 10 which is provided to form an engaging section with a screw thread 11 at its outer side.
- An actuating element 12 formed as a turning/sliding knob, is provided at the proximal end of the shaft 10 and has recesses 13 at its peripheral surface and an arched contact surface 14 at its end face.
- the housing 2 further comprises a section extending downwardly in FIG. 1 and forming a handle 15 , by means of whose upper region 16 the shaft 10 of the piston 5 is led through and which comprises a hollow space 17 in which a locking element. 18 is arranged in a longitudinally displaceable manner.
- the hollow space 17 is formed to be open with respect to the free end of the handle 15 and is closed there with a closing element 19 , for example screwed in.
- the closing element 19 simultaneously serves as a support element for a coil spring 20 with which the locking element 18 is forced into the direction of the upper region 16 of the handle 15 so that it comes into contact with shaft 10 of the piston 5 .
- An unlocking element 21 formed as a slider is connected to the locking element 21 and is displaceably guided in a guide recess 22 at the outer side of the housing 2 .
- the unlocking element is connected to the locking element 18 via a bolt 23 such that when the unlocking element 21 is displaced in the direction of the free end of the handle 15 , the locking element 18 is displaced against the strong force of the spring 20 .
- the flanks 26 , 27 of the screw thread 11 or the teeth 25 which contact one another during the screwing of the piston 5 into the cylinder 3 , are formed to extend substantially perpendicular to the longitudinal axis 6 . It is thus achieved that the high pressure forces created between the flanks 26 and 27 during the screwing of the piston are fully absorbed without a force component acting on the flanks 27 in a direction perpendicular to the longitudinal axis which could effect a displacement of the locking element 18 against the force of the spring 20 . An unwanted uncoupling of the locking element 18 from the shaft 10 is thus excluded even when a very high pressure arises.
- the teeth 25 of the rack 24 are formed in part-annular shape in cross-section and thus create an enlarged contact region with respect to the screw thread 11 . It is thereby ensured that the force occurring between the teeth 25 and the screw thread 11 is spread over the largest possible area so that a breaking out of the teeth 25 or the screw thread 11 is avoided.
- both the unlocking element 21 and the locking element 18 have one bore 28 , 29 each for this purpose into which the respective end of the bolt 23 engages. In this way, a direct coupling is created between the unlocking element 21 and the locking element 18 .
- FIG. 4 shows a cannula formed in accordance with the invention which can, for example, be connected to an apparatus in accordance with FIG. 1.
- the cannula 20 has a coupling element 32 at its proximal end 31 for this purpose which is formed, for example, as a large Luer lock connection and which can be sealingly connected to the corresponding coupling element 9 (see FIG. 1).
- the coupling element is made, for example, of metal in order to be able to absorb the forces which occur when the cannula is driven in.
- Two pin-like handling elements 33 which extend radially outwardly, are provided at the proximal end 31 of the cannula 30 and the inserted cannulae 30 can both be turned simply around their longitudinal axis 34 and simply pulled back out of the body of the patient again in the direction of the longitudinal axis 34 via these.
- a mandrin 35 is shown in FIG. 4 which is inserted in the tube 36 of the cannula 30 and which comprises a closing element 38 at its proximal end 37 .
- the closing element 38 can be used, on the one hand, to hold the mandrin 35 during insertion into and removal from the cannula 30 and, on the other hand, to position the cannula 30 at the desired position using a driving means, for example, a hammer, if required.
- the end face of the closing element 38 is formed as an impact surface 39 for this purpose.
- An aperture 41 is provided at the distal end 40 of the cannula 30 which can be generated, for example, by an oblique cut of the tube 36 .
- the distal end 40 of the cannula 30 is formed asymmetrically with respect to its longitudinal axis 34 by this oblique cut, with in particular the tip 42 of the cannula 30 coming to rest to the side of the longitudinal axis 34 , i.e. at a plane behind the longitudinal axis 34 in the representation of FIG. 4.
- edge 43 of the tube 36 forming the border of the aperture 41 is ground such that this edge 43 forms a cutting edge.
- the mandrin 35 is likewise formed with an oblique cut at its distal end and arranged inside the cannula 30 such that the corresponding oblique surface 44 coincides with the likewise obliquely arranged exit area 45 of the aperture 41 .
- an adjusting unit is provided at the proximal end 37 of the mandrin 35 in the form of a pin 46 which engages into a corresponding recess at the coupling element 32 and thus forms rotational security between the mandrin 35 and the cannula 30 .
- the pin 46 can be seen in more detail in the detailed representation of FIG. 5.
- the arrangement of the mandrin 35 inside the tube 36 of the cannula 30 can likeweise be seen from this representation.
- the closing element 38 has a lug 47 which engages in a hollow space 48 in the coupling element 32 , the diameter of the lug 47 being lower than the clearance of the hollow space 48 so that no jamming of the closing element 38 and thus of the mandrin 35 with the coupling element 32 can take place despite the high impact forces even when the cannula 30 is driven in with a hammer. It is thereby ensured that the mandrin 35 can be removed without problem after the cannula 30 has been positioned.
- the closing element 38 is supported at the end face 50 of the coupling element 32 via a support surface 49 to transmit the impact forces hitting the impact surface 39 of the closing element 38 to the cannula 30 .
- the recess for the pin 46 can generally be formed, for example, as a straight slot extending in the axial direction of the cannula 30
- the recess in FIGS. 6 and 7 is formed as an angled or L-shaped slot 51 .
- the slot 51 comprises a longitudinal section 52 , which extends in the axial direction of the cannula 30 and which forms the open end of the slot 51 at the annular front surface 50 of the coupling element 32 , and a cross-section 53 which extends in the peripheral direction of the coupling element 32 and which is arranged substantially perpendicular to the longitudinal section 52 .
- the slot 51 forms a bayonet fastening together with the pin 46 , with a recess being provided in the form of a latch cutout 55 disposed towards the front face 50 of the coupling element 32 in the region of the free end 54 of the slot 51 and with the pin 46 coming to rest in full or in part therein, depending on the depth of the latch cutout 55 , when the bayonet fastener is closed.
- rotational security of the mandrin 35 is ensured with respect to the cannula 30 despite the cross-section 53 extending in the peripheral direction of the coupling element 32 .
- the cannula 30 is first introduced into the body of the patient together with the inserted mandrin 35 , with this being done with the aid of a hammer where required.
- the coupling between the mandrin 35 and the cannula 30 is made via the bayonet fastening formed by the pin 46 and the slot 51 .
- the bayonet fastening prevents the mandrin 35 from being forced back and partly exiting the cannula 30 due to a spring effect of the mandrin 35 when the cannula 30 is driven in.
- the mandrin 35 could be forced so far back without an appropriate security that the pin 46 would leave its longitudinal guide and that thereby the rotational security would no longer apply between the mandrin 35 and the cannula 30 .
- the respective position of the cannula 30 is tracked during the introduction on a CT (computer tomograph) for example. If the position of the distal end 40 of the cannula 30 deviates from the desired position, the cannula 30 is turned via the handling elements 33 so that the tip 42 comes to lie in the direction of the desired position. In a further introduction of the cannula 30 , a desired migration of this tip 42 in the direction of the desired position will take place due to the asymmetrical tip 42 .
- CT computer tomograph
- the mandrin 35 is gripped via the closing element 38 and optionally pulled out of the cannula 30 after the release of the bayonet fastening.
- the bone cement used is subsequently mixed and sucked into the inside 4 of the cylinder 3 via a loading cannula connected to the coupling element 9 of the application apparatus 1 .
- the unlocking element is downwardly displaced against the force of the spring 20 for this purpose so that the teeth 25 disengage from the screw thread 11 so that the bone cement is sucked into the cylinder 3 via the loading cannula by a simple pulling back of the piston 5 with the shaft 11 .
- the loading cannula is subsequently separated from the application device 1 and the latter is connected to the injection cannula 30 in accordance with the invention which has already been positioned.
- the unlocking element 21 is released so that the locking element 18 is displaced in the direction of the shaft 10 by the force of the spring 20 until the teeth 25 are in engagement with the screw thread 11 .
- the pressure at the inside 4 of the cylinder 3 can subsequently be further increased by turning the shaft 10 via the actuating element 12 so that the piston 5 is slowly further displaced into the inside of the cylinder 1 . If it is recognized, for example by observation at a fluoroscope, that the applied bone cement is flowing in an unwanted direction, this direction of flow can be changed, for example, by the cannula 30 being rotated via the handling elements 33 such that the aperture is disposed in the desired direction.
- the pressure can subsequently be built up again, first by direct displacement and subsequently, as described, by a further screw movement after a reorientation of the cannula 30 , for example, by turning via the handling elements 33 .
- the application apparatus 1 can be separated from the cannula 30 .
- the cannula 30 can subsequently be easily tilted and simultaneously turned around its longitudinal axis 34 with the aid of the handling elements 33 , with a shearing off of the hardened bone cement still located inside the tube 36 taking place due to the oblique, ground edge 43 so that this material is reliably removed from the body together with the cannula 30 when the cannula 30 is subsequently pulled out.
Abstract
An apparatus for the application of bone cement is described having a housing that comprises a cylinder for the reception of the bone cement. The apparatus further comprises a piston arranged in a longitudinally displaceable manner in the cylinder, by which the bone cement can be pressed out of an exit aperture formed in the cylinder, wherein the piston is longitudinally displaceable in the cylinder by a screw movement to apply the bone cement under high pressure. The apparatus can be switched between the displacement of the piston by the screw movement and a direct displacement in the longitudinal direction without a screw movement. Furthermore, a cannula for such an apparatus is described.
Description
- The present invention relates to an apparatus for the application of bone cement having a housing which comprises a cylinder for the reception of the bone cement and having a piston arranged longitudinally displaceably in the cylinder by which the bone cement can be pressed out of an exit aperture formed in the cylinder, with the piston for the application of the bone cement under high pressure being longitudinally displaceable by a screw movement in the cylinder. A cannula for an apparatus for the application of bone cement having an aperture formed at the distal end and a coupling section provided at the proximal end for coupling to the application apparatus is further described.
- Application apparatuses of this kind are used when bone structures break down or become brittle, for example due to bone cancer or osteoporosis. With appropriate apparatuses, the application of bone cement directly into the affected bone structures is possible, whereby these are solidified.
- A plurality of demands must be considered during application. On the one hand, the filling of the application apparatus and the application into the affected bone structures must take place very rapidly, within a few minutes, since the bone cements usually used begin to harden 6 to 7 minutes after mixing. On the other hand, the bone cement must be applied at a very high pressure, since otherwise sufficient penetration of the bone structures is not ensured. Finally, the application of the bone cement must be easily controllable, since a misdirecting of the bone cement can lead to irreversible damage, for example to nerves, particularly during application in the region of the spinal column.
- It is an object of the present invention to provide an apparatus for the application of bone cement and a cannula for an application apparatus, with which the application can be carried out in a short time, with the required high pressure being able to be built up simultaneously and with a control capability of the applied bone cement being possible.
- This object is satisfied in accordance with the invention, starting from an application apparatus of the kind initially named, by the apparatus being switchable between the displacement of the piston by the screw movement and a direct displacement in the longitudinal direction without a screw movement. A cannula in accordance with the invention is characterized in that the distal end of the cannula is formed asymmetrically with a tip disposed to the side of the central axis and in that laterally outwardly projecting handling elements are provided at the proximal end of the cannula with which the cannula can be both turned around its longitudinal axis and displaced along its longitudinal axis.
- Within the framework of this application, the term “proximal” is used in the meaning of “disposed toward the body of the physician”. The term “distal” is used accordingly to mean “disposed remote from the body of the physician”.
- The switchability of the application apparatus in accordance with the invention means that it is possible, for example, for the filling of the cylinder to take place in a very short time by a loading movement of the piston, i.e. by a direct displacement of the piston in the longitudinal direction. The liquid cement present in the cylinder can, vice versa, subsequently be applied in a short time by a direct displacement of the piston for so long until the counter pressure which is created becomes so large that it can no longer be overcome by the direct advance movement. At this moment, the application apparatus is switched to a mode “displacement of the piston by screw movement”, since a substantially greater pressure can be exerted on the piston, and thus on the bone cement to be applied by the screw movement, than with a direct advance movement.
- The advance speed is actually much lower with the screw movement than with a direct displacement in a longitudinal direction; since, however, both the filling of the cylinder and the application of the liquid bone cement can take place in a very short time until the described high pressure is reached due to the direct longitudinal displacement of the piston, there is normally still sufficient time available at that moment when it becomes necessary to switch to the further application by a screw movement to end the application before the bone cement starts to harden.
- A further advantage of the application apparatus formed in accordance with the invention lies in the fact that the high pressure built up during the application with a screw movement can be built up very fast, i.e. within fractions of a second. This is required, for example, when a misdirecting of the bone cement is recognized during the observation, for example at a fluoroscope, of the bone cement exiting the cannula. In this case, a simple switching of the apparatus to the direct longitudinal displaceability of the piston allows the piston to be pushed back due to the high pressure and thus the pressure to be automatically reduced. In this way, the misdirected exit of the bone cement from the distal end of the cannula is stopped directly.
- In accordance with an advantageous embodiment of the invention, the piston comprises an engaging section with a screw thread which engages into a cooperating toothed arrangement provided at the housing so that the longitudinal displacement of the piston takes place when the engaging section is turned. The cooperating toothed arrangement can in particular be formed as a rack. In this way, a very simple, low-cost and reliably working design of an application device in accordance with the invention can be achieved. In particular, a direct displacement in the longitudinal direction is automatically prevented in the operating mode “displacement by screw movement” by the toothed arrangements, which engage into one another, so that the increase of the applied pressure achieved with each revolution is automatically ensured.
- In accordance with a further preferred embodiment of the invention, the screw thread and the cooperating toothed arrangement can be uncoupled, with the cooperating toothed arrangement advantageously being able to be moved substantially perpendicular to the direction of displacement of the piston between a locking position and releasing position for the uncoupling. A simple and fast switch from the operating state “displacement by screw movement” into the operating state “direct displacement in the longitudinal direction” and back is made possible by this design, by, for example, the cooperating toothed arrangement being displaced into the release position via an actuating unit attached to the housing.
- The cooperating toothed arrangement is advantageously pressed against the screw thread under bias. It is ensured in this way that the built-up pressure is automatically ensured for so long until the cooperating toothed arrangement is moved against the bias. This bias can be effected for example by a loading of a spring.
- In accordance with a further advantageous embodiment of the invention, the cooperating toothed arrangement grips around the screw thread regionally, in particular free of undercutting. An enlarged contact surface between the teeth of the cooperating toothed arrangement contacting one another under high pressure and the thread section of the screw thread is achieved by a regional gripping around of the screw thread so that the stability of the apparatus is increased. The gripping around free of undercutting ensures that a simple uncoupling of the screw thread and the cooperating toothed arrangement is still possible, for example by a simple lateral displacement of the cooperating toothed arrangement.
- The piston is preferably substantially freely longitudinally displaceable in the cylinder in the uncoupled state. The free displaceability of the piston is essentially only impaired by a seal which is usually provided for sealing between the piston circumference and the inner wall of the cylinder.
- In accordance with a further advantageous embodiment of the invention, the tooth flanks of the cooperating toothed arrangement and/or the flanks of the thread section of the screw thread which abut one another during the application of the bone cement under pressure form an angle of less than or equal to 90° with the longitudinal axis of the engaging section extending parallel to the direction of displacement. It is ensured by his special formation of the flanks that no overlatching of individual teeth occurs—such as can be the case with normal, chamfered flanks where the angle between the longitudinal axis of the engaging section is greater than 90°—even when very high pressures are used. If the angle amounts to substantially equal to 90°, the cooperating toothed arrangement can be displaced by a displacement movement perpendicular to the direction of movement of the engaging section for the uncoupling from the screw thread. If the angles are less than 90°, uncoupling is possible by a corresponding displacement of the cooperating toothed arrangement obliquely to the longitudinal axis of the engaging section.
- The piston and the engaging section are preferably formed in one piece. With a one-piece formation, it must be ensured that the piston is rotatable in the cylinder in order to allow the screwing of the engaging section in this manner. In this embodiment, the longitudinal displacement of the piston is thus directly achieved by screwing in the piston.
- It is also possible for the piston to be formed in two parts so that the engaging section forms a separate part. In this case, both parts are connected to one another, in particular in a manner rotatable against one another. In this embodiment, it is possible for only the engaging section to be rotated in the screw movement, while the piston is forwardly displaced inside the cylinder without rotation by the forward-screwing engaging section. While in this case the cross-section areas of the piston and the cylinder are complementary to one another, but can be of any shape in principle; for example, they can have an oval or polygonal shape, with the single-piece design of the piston and the engaging section, the cylinder is usually formed as a circular cylinder in order to allow a rotation of the piston in the cylinder together with the engaging section in this manner.
- In accordance with a further advantageous embodiment of the invention, a cannula is fastenable to the exit aperture of the cylinder. This cannula is preferably releasably fastened since, in this way, the cannula can be introduced and positioned in the patient in a first process step without an application apparatus, while the application apparatus can be filled with the liquid bone cement in a second process step only after the successful positioning, for example via a loading cannula likewise attachable to the exit aperture. After the removal of the loading cannula, the application apparatus can subsequently be fastened to the already inserted injection cannula and the bone cement applied in the previously described manner.
- The cannula in accordance with the invention has the advantage that as a result of its asymmetrical tip and also the laterally outwardly projecting handling elements, an exact positioning can already be made during the introduction of the cannula. Conventional cannulae have a symmetrical tip and cannot be altered with respect to their direction of introduction during introduction. With the cannula of the invention, however, the asymmetrical tip can be positioned by a rotation of the partly introduced cannula via the laterally outwardly projecting handling elements such that a movement of the cannula in the desired direction is achieved during the further introduction. The cannula will always deviate slightly in the lateral direction to which the tip is just disposed due to the preceding asymmetrical tip. By a repeated alternate introduction and rotation, an improved positioning and a subsequent correcting of the position is thus still possible during the introduction with the cannula formed in accordance with the invention.
- It is furthermore possible with the cannula of the invention to allow turning or shearing off of the bone cement still hardening inside the cannula from the bone cement applied into the bone structure by turning the cannula still located in the body around its longitudinal access via the handling elements after the hardening of the applied bone cement. It is thereby ensured that the bone cement located inside the cannula remains in it when it is pulled out and is reliably removed from the tissue together with it.
- The edge of the cannula forming the border of the aperture is preferably ground as a cutting edge. A reliable shearing off of the material disposed inside the cannula is thereby also ensured with a completely hardened bone cement.
- In accordance with a further advantageous embodiment of the invention, the penetration surface of the aperture extends obliquely to the longitudinal axis of the cannula. The direction of movement of the bone cement exiting from the aperture in the cannula tip can be controlled in this way. The aperture can be positioned by rotating the cannula via the handling elements such that the exiting material flows in the desired direction. With cannulae having a central aperture, such as are known from the prior art, the bone cement, however, always exists forwardly in a longitudinal direction so that the direction of exit cannot be altered by rotating the cannula.
- Further advantageous embodiments of the invention are given in the dependent claims.
- The invention is described in more detail in the following by way of an embodiment with reference to the drawings, in which are shown:
- FIG. 1 a partly cut-open cross-section of an application apparatus formed in accordance with the invention;
- FIG. 2 a detailed view of an apparatus of FIG. 1;
- FIG. 3 a partly cut-open cross-section of the apparatus of FIG. 1;
- FIG. 4 a cannula formed in accordance with the invention;
- FIG. 5 a detailed view of the cannula of FIG. 4;
- FIG. 6 a further embodiment of a cannula formed in accordance with the invention; and
- FIG. 7 a detailed view of the cannula of FIG. 6.
- FIG. 1 shows a pistol-like application apparatus1 having a housing 2 whose central region is formed as a cylinder 3 for the reception of bone cement at its inside 4. A
piston 5 is displaceably supported in the direction of itslongitudinal axis 6 inside the cylinder 3, with thepiston 5 being sealed with respect to the inner wall of the cylinder 3 by a sealing means 7. An exit aperture 8 is formed at the distal end of the cylinder 3 and coupling element 9, formed for example as a large Luer lock connection, is provided thereat for the coupling of a cannula. - The
piston 5 is formed in one piece with anelongated shaft 10 which is provided to form an engaging section with a screw thread 11 at its outer side. Anactuating element 12, formed as a turning/sliding knob, is provided at the proximal end of theshaft 10 and hasrecesses 13 at its peripheral surface and anarched contact surface 14 at its end face. - The housing2 further comprises a section extending downwardly in FIG. 1 and forming a
handle 15, by means of whoseupper region 16 theshaft 10 of thepiston 5 is led through and which comprises ahollow space 17 in which a locking element. 18 is arranged in a longitudinally displaceable manner. - The
hollow space 17 is formed to be open with respect to the free end of thehandle 15 and is closed there with aclosing element 19, for example screwed in. The closingelement 19 simultaneously serves as a support element for acoil spring 20 with which thelocking element 18 is forced into the direction of theupper region 16 of thehandle 15 so that it comes into contact withshaft 10 of thepiston 5. - An unlocking
element 21 formed as a slider is connected to the lockingelement 21 and is displaceably guided in aguide recess 22 at the outer side of the housing 2. The unlocking element is connected to the lockingelement 18 via abolt 23 such that when the unlockingelement 21 is displaced in the direction of the free end of thehandle 15, the lockingelement 18 is displaced against the strong force of thespring 20. - The cooperation of the locking
element 18 with theshaft 10 of thepiston 5 is shown more clearly in FIG. 2. - It can be seen in FIG. 2, that the end of the locking
element 18 dispose, toward theshaft 10 is formed as arack 24 whoseteeth 25 form a cooperating toothed arrangement for the screw thread 11 of theshaft 10. - If the unlocking
element 21 is displaced downwardly to the free end of thehandle 15, then the lockingelement 18 is displaced downwardly against the force of thespring 20 via thebolt 23 until the lockingelement 18 and theshaft 10 are uncoupled, as is shown in FIG. 2. In this state, theshaft 10, and thus thepiston 5, can be substantially freely displaced directly in the longitudinal direction in the cylinder 3 by, for example, pressing the palm of the hand on thecontact surface 14. This displaceability is slightly impaired only by the friction present between the sealing means 7 and the inner wall of the cylinder 3. - If the unlocking
element 21 is released again, the lockingelement 18 is forced in the direction of theshaft 10 by the force of thespring 20 until theteeth 25 of therack 24 come into engagement with the screw thread 11 of theshaft 10. In this state, a longitudinal displacement of theshaft 10, and thus of thepiston 5, is only possible by a screwing of theshaft 10, with this preferably being carried out via theactuating element 12 formed as a screw head. While, in this state, only a relatively slight advance of thepiston 5 is carried out by the screw movement in each case, the pressure which can be applied to the bone cement arranged at the inside 4 of the cylinder 3 by the screw movement is, however, substantially higher than can be generated by a direct displacement in the longitudinal direction of theshaft 10 with theshaft 10 uncoupled from the lockingelement 18. - As can be seen from FIG. 2, the
flanks teeth 25, which contact one another during the screwing of thepiston 5 into the cylinder 3, are formed to extend substantially perpendicular to thelongitudinal axis 6. It is thus achieved that the high pressure forces created between theflanks flanks 27 in a direction perpendicular to the longitudinal axis which could effect a displacement of the lockingelement 18 against the force of thespring 20. An unwanted uncoupling of the lockingelement 18 from theshaft 10 is thus excluded even when a very high pressure arises. - It can be seen from the part cross-section of FIG. 3 that the
teeth 25 of therack 24 are formed in part-annular shape in cross-section and thus create an enlarged contact region with respect to the screw thread 11. It is thereby ensured that the force occurring between theteeth 25 and the screw thread 11 is spread over the largest possible area so that a breaking out of theteeth 25 or the screw thread 11 is avoided. - Furthermore, the coupling of the locking
element 18 with the unlockingelement 21 via thebolt 23 can be seen in FIG. 3. Both the unlockingelement 21 and the lockingelement 18 have onebore bolt 23 engages. In this way, a direct coupling is created between the unlockingelement 21 and the lockingelement 18. - FIG. 4 shows a cannula formed in accordance with the invention which can, for example, be connected to an apparatus in accordance with FIG. 1. The
cannula 20 has acoupling element 32 at itsproximal end 31 for this purpose which is formed, for example, as a large Luer lock connection and which can be sealingly connected to the corresponding coupling element 9 (see FIG. 1). The coupling element is made, for example, of metal in order to be able to absorb the forces which occur when the cannula is driven in. - Two pin-
like handling elements 33, which extend radially outwardly, are provided at theproximal end 31 of thecannula 30 and the insertedcannulae 30 can both be turned simply around theirlongitudinal axis 34 and simply pulled back out of the body of the patient again in the direction of thelongitudinal axis 34 via these. - Furthermore, a
mandrin 35 is shown in FIG. 4 which is inserted in thetube 36 of thecannula 30 and which comprises aclosing element 38 at itsproximal end 37. The closingelement 38 can be used, on the one hand, to hold themandrin 35 during insertion into and removal from thecannula 30 and, on the other hand, to position thecannula 30 at the desired position using a driving means, for example, a hammer, if required. The end face of theclosing element 38 is formed as animpact surface 39 for this purpose. - An aperture41 is provided at the distal end 40 of the
cannula 30 which can be generated, for example, by an oblique cut of thetube 36. The distal end 40 of thecannula 30 is formed asymmetrically with respect to itslongitudinal axis 34 by this oblique cut, with in particular the tip 42 of thecannula 30 coming to rest to the side of thelongitudinal axis 34, i.e. at a plane behind thelongitudinal axis 34 in the representation of FIG. 4. - The edge43 of the
tube 36 forming the border of the aperture 41 is ground such that this edge 43 forms a cutting edge. - The
mandrin 35 is likewise formed with an oblique cut at its distal end and arranged inside thecannula 30 such that thecorresponding oblique surface 44 coincides with the likewise obliquely arrangedexit area 45 of the aperture 41. To ensure this coincidence, an adjusting unit is provided at theproximal end 37 of themandrin 35 in the form of apin 46 which engages into a corresponding recess at thecoupling element 32 and thus forms rotational security between themandrin 35 and thecannula 30. - The
pin 46 can be seen in more detail in the detailed representation of FIG. 5. The arrangement of themandrin 35 inside thetube 36 of thecannula 30 can likeweise be seen from this representation. - The
closing element 38 has alug 47 which engages in ahollow space 48 in thecoupling element 32, the diameter of thelug 47 being lower than the clearance of thehollow space 48 so that no jamming of theclosing element 38 and thus of themandrin 35 with thecoupling element 32 can take place despite the high impact forces even when thecannula 30 is driven in with a hammer. It is thereby ensured that themandrin 35 can be removed without problem after thecannula 30 has been positioned. - The
closing element 38 is supported at theend face 50 of thecoupling element 32 via asupport surface 49 to transmit the impact forces hitting theimpact surface 39 of theclosing element 38 to thecannula 30. - While the recess for the
pin 46 can generally be formed, for example, as a straight slot extending in the axial direction of thecannula 30, the recess in FIGS. 6 and 7 is formed as an angled or L-shapedslot 51. Theslot 51 comprises alongitudinal section 52, which extends in the axial direction of thecannula 30 and which forms the open end of theslot 51 at the annularfront surface 50 of thecoupling element 32, and across-section 53 which extends in the peripheral direction of thecoupling element 32 and which is arranged substantially perpendicular to thelongitudinal section 52. - The
slot 51 forms a bayonet fastening together with thepin 46, with a recess being provided in the form of alatch cutout 55 disposed towards thefront face 50 of thecoupling element 32 in the region of thefree end 54 of theslot 51 and with thepin 46 coming to rest in full or in part therein, depending on the depth of thelatch cutout 55, when the bayonet fastener is closed. In this way, rotational security of themandrin 35 is ensured with respect to thecannula 30 despite thecross-section 53 extending in the peripheral direction of thecoupling element 32. - The application apparatus1 in accordance with the invention and the cannula formed in accordance with the invention are used as follows:
- The
cannula 30 is first introduced into the body of the patient together with the insertedmandrin 35, with this being done with the aid of a hammer where required. In the embodiment of FIGS. 6 and 7, the coupling between themandrin 35 and thecannula 30 is made via the bayonet fastening formed by thepin 46 and theslot 51. The bayonet fastening prevents the mandrin 35 from being forced back and partly exiting thecannula 30 due to a spring effect of themandrin 35 when thecannula 30 is driven in. Themandrin 35 could be forced so far back without an appropriate security that thepin 46 would leave its longitudinal guide and that thereby the rotational security would no longer apply between themandrin 35 and thecannula 30. - The respective position of the
cannula 30 is tracked during the introduction on a CT (computer tomograph) for example. If the position of the distal end 40 of thecannula 30 deviates from the desired position, thecannula 30 is turned via thehandling elements 33 so that the tip 42 comes to lie in the direction of the desired position. In a further introduction of thecannula 30, a desired migration of this tip 42 in the direction of the desired position will take place due to the asymmetrical tip 42. - When the
cannula 30 is correctly positioned, themandrin 35 is gripped via theclosing element 38 and optionally pulled out of thecannula 30 after the release of the bayonet fastening. - The bone cement used is subsequently mixed and sucked into the inside4 of the cylinder 3 via a loading cannula connected to the coupling element 9 of the application apparatus 1. The unlocking element is downwardly displaced against the force of the
spring 20 for this purpose so that theteeth 25 disengage from the screw thread 11 so that the bone cement is sucked into the cylinder 3 via the loading cannula by a simple pulling back of thepiston 5 with the shaft 11. - The loading cannula is subsequently separated from the application device1 and the latter is connected to the
injection cannula 30 in accordance with the invention which has already been positioned. - In the next process step, again with an
uncoupled locking element 18, thepiston 5 is pushed directly into the cylinder 1 with theshaft 10 by pressure loading of thecontact surface 14 of theactuating element 12, whereby the cement material arranged at the inside 4 of the cylinder 3 is injected into the bone via thecannula 30. A constantly increasing pressure is built up by the injection into the bone material until said pressure is finally so high that a further application of the bone cement by pressing onto thecontact surface 14 is no longer possible. - At this point in time, the unlocking
element 21 is released so that the lockingelement 18 is displaced in the direction of theshaft 10 by the force of thespring 20 until theteeth 25 are in engagement with the screw thread 11. - The pressure at the inside4 of the cylinder 3 can subsequently be further increased by turning the
shaft 10 via theactuating element 12 so that thepiston 5 is slowly further displaced into the inside of the cylinder 1. If it is recognized, for example by observation at a fluoroscope, that the applied bone cement is flowing in an unwanted direction, this direction of flow can be changed, for example, by thecannula 30 being rotated via thehandling elements 33 such that the aperture is disposed in the desired direction. - If the quantity of bone cement exiting the aperture41 is too high due to the high pressure, then this pressure can be reduced immediately by a displacement of the unlocking
element 21 and the uncoupling and release which thereby takes place of theshaft 10 and thepiston 5 connected thereto. It is prevented in this manner that the bone cement is applied to dangerous points inside the body. - The pressure can subsequently be built up again, first by direct displacement and subsequently, as described, by a further screw movement after a reorientation of the
cannula 30, for example, by turning via thehandling elements 33. - After the full application of the bone cement, the application apparatus1 can be separated from the
cannula 30. - After hardening, the
cannula 30 can subsequently be easily tilted and simultaneously turned around itslongitudinal axis 34 with the aid of thehandling elements 33, with a shearing off of the hardened bone cement still located inside thetube 36 taking place due to the oblique, ground edge 43 so that this material is reliably removed from the body together with thecannula 30 when thecannula 30 is subsequently pulled out. -
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Claims (30)
1. An apparatus for the application of bone cement having a housing which comprises a cylinder for the reception of the bone cement and having a piston arranged in a longitudinally displaceable manner in the cylinder by which the bone cement can be pressed out through an exit aperture formed in the cylinder, a screw movement for longitudinally displacing the piston in the cylinder for the application of the bone cement under high pressure, and an arrangement for switching between the displacement of the piston by the screw movement and a direct displacement in the longitudinal direction without a screw movement.
2. An apparatus in accordance with claim 1 , wherein the piston comprises an engaging section having a screw thread that engages into a cooperating toothed arrangement provided at the housing such that the longitudinal displacement of the piston is effected when the engaging section is turned.
3. An apparatus in accordance with claim 2 , wherein the cooperating toothed arrangement is formed as a rack.
4. An apparatus in accordance with claim 2 , wherein the screw thread and the cooperating toothed arrangement can be uncoupled.
5. An apparatus in accordance with claim 4 , characterized in that the cooperating toothed arrangement can be moved in a direction substantially perpendicular to the direction of displacement of the piston for the uncoupling.
6. An apparatus in accordance with claim 2 , wherein the cooperating toothed arrangement is pressed against the screw thread under bias.
7. An apparatus in accordance with claim 2 , wherein the cooperating toothed arrangement grips around the screw thread regionally.
8. An apparatus in accordance with claim 7 , wherein the cooperating toothed arrangement grips around the screw thread regionally free of undercutting.
9. An apparatus in accordance with claim 4 , wherein the piston can be longitudinally displaced in a substantially free manner in the cylinder when uncoupled.
10. An apparatus in accordance with claim 2 , wherein tooth flanks of the cooperating toothed arrangement and/or flanks of the thread section of the screw thread, which contact one another during the application of the bone cement form under pressure, form an angle of less than or equal to approximately 90° with the longitudinal axis of the engaging section which extends parallel to the direction of displacement.
11. An apparatus in accordance with claim 2 , wherein the other tooth flanks of the cooperating toothed arrangement and/or the other flank of the thread section of the screw thread form an angle of more than approximately 90° with the longitudinal axis of the engaging section which extends parallel to the direction of displacement.
12. An apparatus in accordance with claim 2 , wherein the piston and the engaging section are formed as one piece.
13. An apparatus in accordance with claim 2 , wherein the piston and the engaging section are formed as separate parts which are connected to one another and which are in particular rotatable with respect to one another.
14. An apparatus in accordance with claim 1 , wherein the cylinder comprises a circular cylinder.
15. An apparatus in accordance with claim 1 , wherein a cannula can be fastened to the exit aperture of the cylinder.
16. An apparatus in accordance with claim 15 comprising a cannula according to claim 17 .
17. A cannula for an apparatus for the application of bone cement having an aperture formed at a distal end and a coupling section provided at a proximal end for the coupling to the application apparatus, wherein the distal end of the cannula is formed asymmetrically with a tip disposed to the side of the longitudinal axis; and handling elements projecting outwardly to the side are provided at the proximal end of the cannula with which the cannula can both be rotated around a longitudinal axis thereof and displaced along a longitudinal direction.
18. A cannula in accordance with claim 17 for an application apparatus in accordance with claim 1 .
19. A cannula in accordance with claim 17 , wherein an edge of the cannula end forming the border of the aperture is ground as a cutting edge.
20. A cannula in accordance with claim 17 , wherein a passage area of the aperture extends obliquely to the longitudinal axis of the cannula.
21. A cannula in accordance with claim 17 , wherein two handling elements are provided which are arranged with respect to the longitudinal axis of the cannula, in particular opposite thereto.
22. A cannula in accordance with claim 17 , the handling elements are formed as pin-like elements projecting radially outwardly.
23. A cannula in accordance with claim 17 , wherein a mandrin can be inserted into the cannula; and a connecting element is provided in the region of the proximal end of the cannula, to generate a connection between the mandrin and the cannula which is releasable, rotationally fixed and/or displaceably fixed in the axial direction.
24. A cannula in accordance with claim 23 , wherein the connecting element is provided at a coupling section of the cannula.
25. A cannula in accordance with claim 23 , wherein a counter element cooperating with the connecting element is provided at the mandrin.
26. A cannula in accordance with claim 25 , wherein the counter element is provided in a region of the proximal end of the mandrin.
27. A cannula in accordance with claim 23 , wherein the connection between the mandrin and the cannula comprises a bayonet fastening.
28. A cannula in accordance with claim 23 , wherein the connecting element is formed as a slot-like recess, in particular as a groove or breakthrough, and the counter element is formed in particular as a pin-like lug or vice versa.
29. A cannula in accordance with claim 28 , wherein the recess comprises at least one longitudinal section extending in the axial direction of the cannula.
30. A cannula in accordance with claim 29 , wherein a cross-section of the recess extending in a peripheral direction of the cannula connects to the longitudinal section.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/038,798 US7883512B2 (en) | 2000-05-25 | 2005-01-20 | Apparatus for the application of bone cement |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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DE10025898.0 | 2000-05-25 | ||
DE10025898 | 2000-05-25 | ||
DE10064202.0 | 2000-12-22 | ||
DE10064202A DE10064202A1 (en) | 2000-05-25 | 2000-12-22 | Device for applying bone cement and cannula for such a device |
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US11/038,798 Continuation US7883512B2 (en) | 2000-05-25 | 2005-01-20 | Apparatus for the application of bone cement |
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US20020013553A1 true US20020013553A1 (en) | 2002-01-31 |
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ID=26005832
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US09/865,109 Abandoned US20020013553A1 (en) | 2000-05-25 | 2001-05-24 | Apparatus for the application of bone cement and a cannula for such an apparatus |
US11/038,798 Active 2025-09-07 US7883512B2 (en) | 2000-05-25 | 2005-01-20 | Apparatus for the application of bone cement |
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Application Number | Title | Priority Date | Filing Date |
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US11/038,798 Active 2025-09-07 US7883512B2 (en) | 2000-05-25 | 2005-01-20 | Apparatus for the application of bone cement |
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US (2) | US20020013553A1 (en) |
EP (2) | EP1726274B1 (en) |
AT (2) | ATE390102T1 (en) |
DE (4) | DE10064202A1 (en) |
DK (2) | DK1726274T3 (en) |
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PT (2) | PT1726274E (en) |
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Also Published As
Publication number | Publication date |
---|---|
PT1157677E (en) | 2007-04-30 |
EP1157677B1 (en) | 2007-02-14 |
ES2282168T5 (en) | 2012-10-16 |
ATE390102T1 (en) | 2008-04-15 |
DE20122395U1 (en) | 2005-08-18 |
US20050124997A1 (en) | 2005-06-09 |
ATE353611T1 (en) | 2007-03-15 |
EP1726274A1 (en) | 2006-11-29 |
DE10064202A1 (en) | 2001-11-29 |
US7883512B2 (en) | 2011-02-08 |
DK1157677T4 (en) | 2012-06-25 |
DE50113802D1 (en) | 2008-05-08 |
ES2282168T3 (en) | 2007-10-16 |
PT1726274E (en) | 2008-05-19 |
ES2301124T3 (en) | 2008-06-16 |
EP1157677A3 (en) | 2002-02-06 |
DE50112023D1 (en) | 2007-03-29 |
EP1157677A2 (en) | 2001-11-28 |
DK1157677T3 (en) | 2007-04-23 |
DK1726274T3 (en) | 2008-07-21 |
EP1726274B1 (en) | 2008-03-26 |
EP1157677B2 (en) | 2012-05-23 |
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