WO2013025448A1 - Remplacement de corps vertébral - Google Patents

Remplacement de corps vertébral Download PDF

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Publication number
WO2013025448A1
WO2013025448A1 PCT/US2012/050218 US2012050218W WO2013025448A1 WO 2013025448 A1 WO2013025448 A1 WO 2013025448A1 US 2012050218 W US2012050218 W US 2012050218W WO 2013025448 A1 WO2013025448 A1 WO 2013025448A1
Authority
WO
WIPO (PCT)
Prior art keywords
endplate
implant
expandable body
core
vertebral body
Prior art date
Application number
PCT/US2012/050218
Other languages
English (en)
Inventor
Shaeffer BANNIGAN
Ryan Donahoe
Original Assignee
Nuvasive, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nuvasive, Inc. filed Critical Nuvasive, Inc.
Publication of WO2013025448A1 publication Critical patent/WO2013025448A1/fr
Priority to US14/177,100 priority Critical patent/US9687357B2/en
Priority to US15/635,087 priority patent/US10390960B2/en
Priority to US16/510,123 priority patent/US11458025B2/en
Priority to US17/822,877 priority patent/US20220401228A1/en

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Classifications

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    • A61F2/44—Joints for the spine, e.g. vertebrae, spinal discs
    • A61F2/4455—Joints for the spine, e.g. vertebrae, spinal discs for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages
    • A61F2/4465—Joints for the spine, e.g. vertebrae, spinal discs for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages having a circular or kidney shaped cross-section substantially perpendicular to the axis of the spine
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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
    • A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005—The prosthesis being constructed from a particular material
    • A61F2310/00011—Metals or alloys
    • A61F2310/00017—Iron- or Fe-based alloys, e.g. stainless steel
    • 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
    • A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005—The prosthesis being constructed from a particular material
    • A61F2310/00011—Metals or alloys
    • A61F2310/00023—Titanium or titanium-based alloys, e.g. Ti-Ni alloys

Definitions

  • the present invention relates generally to spinal implants.
  • the spine is formed of a column of vertebra that extends between the cranium and pelvis.
  • the three major sections of the spine are known as the cervical, thoracic and lumbar regions.
  • a series of about 9 fused vertebrae extend from the lumbar region of the spine and make up the pelvic region of the vertebral column. These fused vertebrae consist of the sacral and coccygeal region of the vertebral column.
  • the main functions of the spine are to provide skeletal support and protect the spinal cord. Even slight disruptions to either the intervertebral discs or vertebrae can result in serious discomfort due to compression of nerve fibers either within the spinal cord or extending from the spinal cord. If a disruption to the spine becomes severe enough, damage to a nerve or part of the spinal cord may occur and can result in partial to total loss of bodily functions (e.g. walking, talking, and breathing). Therefore, it is of great interest and concern to be able to both correct and prevent any ailments of the spine. Trauma to the spine (e.g. car accident, sports injury) can cause fracturing of one or more vertebrae. Certain diseases affecting the spine (e.g. tumors, osteoporosis) can cause degeneration of the spine.
  • the present invention is directed at overcoming, or at least improving upon, the disadvantages of the prior art.
  • Fig. 1 is an exploded view of the vertebral body implant assembly, according to one embodiment of the present invention
  • Fig. 2 is a perspective view of an alternative embodiment of the vertebral body implant assembly
  • Fig. 2A is a cross section view of the vertebral body implant assembly of Fig. 2 taken along lines 2-2 of Fig.2;
  • Fig. 3 is an exploded view of an alternative embodiment of the core expanding body forming part of the implant assembly of Fig. 1;
  • Fig. 4 is an exploded view of an alternative embodiment of the core expanding body forming part of the implant assembly of Fig. 1;
  • Fig. 5 is a perspective view of the core expanding body forming part of the implant assembly of Fig. 1;
  • Fig. 5A is a cross section view of the core expanding body of Fig. 5 taken along lines 5-5 of Fig.5;
  • Fig. 6 is a perspective view of the outer core forming part of the implant assembly of Fig. l;
  • Fig. 7 is a perspective view of an alternative embodiment of the outer core forming part of the implant assembly of Fig. 1;
  • Fig. 8 is a perspective view of an alternative embodiment of the outer core forming part of the implant assembly of Fig. 1;
  • Fig. 9 is a perspective view of the inner core forming part of the implant assembly of Fig. l ;
  • Fig. 10 is a perspective view of an alternative embodiment of the inner core forming part of the implant assembly of Fig. 1;
  • Fig. 11 is a perspective view of an alternative embodiment of the inner core forming part of the implant assembly of Fig. 1;
  • Fig. 12 is a perspective view of the adjustment ring forming part of the implant assembly of Fig. 1;
  • Fig. 12A is a cross section view of the adjustment ring of Fig. 12 taken along lines 12-12 of Fig.12;
  • Fig. 13 is a top view of the endplate forming part of the implant assembly of Fig. 1;
  • Fig. 14 is a top view of an alternative embodiment of the endplate forming part of the implant assembly of Fig. 1;
  • Fig. 15 is a perspective view of the bottom of the endplate of Fig. 13;
  • Fig. 16 is a side view of the endplate of Fig. 13;
  • Fig. 17 is a perspective view of one example of a combined insertion and expansion, according to one embodiment of the present invention.
  • Fig. 18 is a perspective view of the expanding tool of Fig. 17 with the outer cover removed;
  • Fig. 19 is a side view of the adjustment region of the expanding tool of Fig. 17;
  • Fig. 20 is an exploded view of the large bezel forming part of the expanding tool of Fig.
  • Fig. 21 is a cross section view of adjustment region taken along line 18-18 of Fig. 18;
  • Fig. 22 is a cross section view of the distal handle taken along line 18-18 of Fig. 18;
  • Fig. 23 is a cross section view of the proximal engagement region taken along line 18-18 of Fig. 18;
  • Fig. 24 is a perspective view of the proximal engagement region with the outer cover and elongated first shaft removed;
  • Fig. 25 is a side view of the outer cover forming part of the expanding tool of Fig. 17;
  • Fig. 26 is an exploded view of an alternative embodiment of the expanding tool
  • Fig. 27 is a perspective view of the expanding tool of Fig. 26;
  • Fig. 28A-28D is a series of side views of the implant assembly of Fig. 1 engaged with the expanding tool of Fig. 17 and the process of implanting the expandable vertebral body between a first vertebra and second vertebra.
  • FIG. 1 illustrates an example of an expandable vertebral body replacement implant assembly 10 according to a first embodiment.
  • the vertebral body replacement implant assembly 10 includes endplates 11 fixed at the superior and inferior ends of an expanding core body 12 wherein the expandable implant can be customized to accommodate various needs by attaching one from a selection of different endplates.
  • the customization of the expandable core can be done in situ or moments before implantation of the expandable vertebral body replacement, which gives the benefit of customizing the implant based on expected and unexpected circumstances and conditions of the surrounding vertebral bodies.
  • the expanding core body 12 includes an adjustment ring 13, an outer core 14, an inner core 15, one or more guide pins 20, and one or more set screws 16.
  • the vertebral body replacement implant assembly 10 of the present invention may be inserted into a space left by the removal of at least part of one or more vertebra in order to maintain a desired spacing between the remaining vertebrae and to stabilize the affected spinal segments. To do so, the vertebral body replacement implant assembly 10 is placed, preferably in a collapsed state, in the space between the remaining superior and inferior vertebral bodies.
  • Figures 2 and 2A show an alternative embodiment of the vertebral body replacement implant assembly 10.
  • Figure 2A is a cutaway view with the adjustment ring 13 removed for greater detail of the first end 39 of the outer core 15 and the inner core 14.
  • Figure 3 and 4 show exploded views of alternative embodiments of the core expanding body 12. All of the displayed configurations, shown as examples only, may be used without departing from the scope of the invention.
  • the outer core 14 includes indented slots 23, an opening 24, a first end 39, a second end 41, a plurality of flanges 25 with a distal step 26 forming a groove 44, a set screw opening 35, and a specially sized aperture 88.
  • Indented slots 23 on the exterior wall of the outer core 14 allow for the anti-rotational attachment of the expanding tool, described below.
  • the openings 24 in the wall of the outer core 14 allow the transport of blood and nutrients through the core expanding body 12 once implanted, which assists in new bone growth between the remaining vertebra. Larger openings 24 in the side of the outer core 14 allow the placement of additional bone growth promoting material to be added once the vertebral body implant assembly 10 has been positioned in the body and expanded to a desired height.
  • a plurality of flanges 25 with a distal step 26 extend from the first end 39 of the outer core 14 and function to secure the attachment of the adjustment ring 13 to the first end 39.
  • the outer core 14 may have a specially sized aperture 88 directly adjacent to the set screw opening 35 that allows for the insertion of the expanding tool 200, described below.
  • the outer core 14, shown by way of examples in Figures 6 and 8, may include a second end slot 47 and second end groove 46 which allow similarly configured endplates 11 to slide on to the outer core 12 and hold the endplate 11 in place.
  • the connection may be augmented through the use of a endplate attachment screw 90 placed through the endplate hole 62 and in the screw slot flange 68 through to base threaded hole 45 on the second end 41 of the outer core 14.
  • the outer core 14 may have base threaded holes 45 encircling a central aperture at the second end 41 defining a generally sinusoidal or flower-shaped perimeter of the attachment portion.
  • the base threaded holes 45 allow for an endplate 11 to be placed in different rotational positions that provides for additional customization. Though no set configuration or number of base threaded holes 45 is needed to fall within the scope of the invention, in the illustrated embodiment there are 12 threaded holes 45 to allow for attachment of the endplate 11 at 12 different angles relative to the expandable core body 12.
  • the attachment portion of the outer core and corresponding recess in the endplate 11 may be any configuration that allows for placement of the endplate 11 at one of a plurality of angles relative to the outer core 14.
  • the inner surface of the outer core 14 is generally round with 1 or more flat sides. The flat surface contains the set screw opening 35 in which the set screw 16 is placed and tightened to assist in locking the inner core 15 in place.
  • the indented slots 23, best seen in Figure 5, serve to allow secure connection between the core expanding body 12 and the expanding tool 200.
  • the indented slots 23 are placed on the outer core 14 without disrupting the functioning of the adjustment ring 13 or the inner core 15, and may be provided in any number of suitable shapes or dimensions without departing for the scope of the invention.
  • the largest diameter of the outer core 14 is preferably dimensioned to be generally in the range of 12mm to 22mm, respectively.
  • the height of the outer core 14 is preferably dimensioned to be generally in the range of 14mm to 68mm.
  • the height of the expandable core body assembly 12 i.e. endplates not included in the height measurement is preferably dimensioned to be generally in the range of 15mm to 121mm.
  • the adjustment ring 13, shown by way of example in Figures 5 and 6 includes external features 21, internal threads 17, and an annular under-step 18 forming a groove 19.
  • the annular under-step 18 of adjustment ring 13 engages in the groove 41 of the core expanding body 12
  • the distal step 26 engages in the groove 19 of the adjustment ring 13, longitudinally fixing the adjustment ring 13 and core expanding body 12 together while permitting rotational movement therebetween.
  • External features 21 on the adjustment ring 13 are configured to engage a combination inserter/expansion tool which may be operated to rotate adjustment ring 13 to expand core expanding body 12.
  • the internal threads 17 of the adjustment ring 13 engage with the external threads 31 of the inner core 15 so that as the adjustment ring 13 rotates, it acts as a nut and forces the linear translation of the inner core 15 along its central axis.
  • the longitudinal fixation of the outer core 14 to the adjustment ring 13 ensures the relative displacement of the inner core 15 to the outer core 14 as the adjustment ring 13 rotates.
  • the diameter of the adjustment ring 13 is preferably dimensioned generally in the range of 12mm to 22mm.
  • the height of the adjustment ring 13 is preferably dimensioned to be generally in the range of 5mm to 10mm.
  • the inner core 15, illustrated in Figures 9-11, is composed of a first end 40 and a generally elongated body 51 extending from the first end 40, and with at least one generally helical exterior thread 31.
  • One or more guide tracks 19 ingrained into the exterior wall of the body 51 run parallel to the central axis of the body 51.
  • the guide track 19 receives guide pins 20 which extend through the outer core 14.
  • a guide pin 20 travels along a guide track 19, rotationally fixing inner core 15 to outer core 14, while permitting longitudinal movement therebetween.
  • a guide pin 20 may have threaded features that allow it to screw into threaded holes in the wall of the outer core.
  • a central lumen 27 through the inner core 15 enables additional bone growth promoting material to be placed within the expanding core body 12, and ultimately to allow new bone to form uninterrupted through the entire central axis of the vertebral body replacement implant assembly 10.
  • the central lumen 27 may be generally cylindrical in shape (having a generally circular cross-section) or in the alternative may have a cross section having any geometric shape without departing from the scope of the present invention.
  • the inner core 15 may also contain a flat, non-threaded area 49 running some distance vertically along the outer surface.
  • the non-threaded area 49 is designed to fit next to the inner flat surface of the outer core 14.
  • the inner core 15 can be locked in place via the friction created when the set screw 16 is tightened into the non-threaded area 49.
  • the first end 40 of the inner core 15 may have a number of different configurations in which attachment to the endplate 11 is possible.
  • the first end 40 may consist of encircling threaded holes 48 - with the same features as described above for the exemplary configuration of second end 41 on the outer core 14.
  • the threaded holes 48 allow for secure attachment through the use of an endplate attachment screw 90 to attach the inner core 15 to the endplate 11 configured to accept a screw. This arrangement allows for rotational customization of the endplate prior to insertion into the patient.
  • An alternative embodiment for the first end 40 of the inner core 15 includes a side flange 70 and groove 71 best seen in Figure 9.
  • the side flanges 70 and groove 71 are specifically designed to fit with a variation of endplate 11 (as shown, for example, in Figure 15) with matching endplate flanges 69 and endplate grooves 67 by sliding the endplate 11 along the surface of the first end 40 so the flanges on each piece rest within the grooves of the other.
  • the attachment feature of the endplate 11 While shown in Figure 15 with the attachment feature of the endplate 11 configured for insertion of the engagement feature on the inner core 15 parallel to the longitudinal axis of the endplate, it is also contemplated that the attachment feature of the endplate may be configured for insertion of the inner core at an angle oblique to the longitudinal axis.
  • Both the first end 40 and the endplate 11 may contain a hole for the insertion of an endplate attachment screw 90 to lock the endplate 11 in place.
  • This screw connection feature may be accomplished in similar ways without departing from the scope of the patent.
  • the perimeter shape of the first end 40 may be provided in any number of suitable shapes or dimensions without departing from the scope of the invention, provided that the perimeter shape corresponds to the perimeter shape of the attachment features of the endplate 11.
  • the customizable core expanding body 12 can be used in a variety of surgical approaches (e.g. anterior, anterior-lateral, lateral, posterior or posterior-lateral).
  • the customizable core expanding body 12 can be placed in a variety of positions along the spine, and the customizable core expanding body 12 can be made compatible with a variety of conditions of the surrounding vertebral bodies (e.g. partial removal of vertebral body).
  • the vertebral body implant assembly 10 is preferably composed of either metal (e.g. titanium, stainless steel, etc.) or polymer (e.g. poly-ether-ether-ketone (PEEK)).
  • PEEK poly-ether-ether-ketone
  • one or more marker rods 61 are preferably composed of a radiopaque material (e.g. titanium) and are positioned within the vertebral body implant assembly 10 so that the positioning of the vertebral body implant assembly 10 can be visible upon X-ray imaging. This visual indication may be obtained either postoperatively or intra-operatively to confirm placement of the vertebral body implant assembly 10.
  • Figures 13-14 illustrate the second surface 34 of the endplate 11 which includes one or more liner ridges 60, the center hole 62, an anterior side 64, a posterior side 66, lateral sides 65, a screw slot 63, a screw slot flange 68, one or more windows 30, and one or more marker rods 61.
  • the second surface 34 is configured to be positioned against the adjacent vertebral body with the anterior side 64 positioned generally towards the anterior side of the adjacent vertebral body.
  • the generally larger radii corners at the ends of the anterior side 64 are configured to generally conform to the natural shape of the anterior portion of a vertebral body.
  • the endplate 11 is configured for a preferred use through a lateral approach to the spine, and preferably when endplate coverage is desired to span across the ring apophysis of the vertebra.
  • the distance between the two lateral sides 65 has a length dimensioned to extend generally across the space from the apophyseal ring at one lateral aspect of the spine to the apophyseal ring at the other lateral aspect of the spine. This allows the endplate 11 to provide more support and distribute the weight more evenly throughout the adjacent vertebral body, which lessens stress and potential damage to the adjacent vertebral body.
  • the ridges 60 provide additional placement stabilization and are shown in this embodiment to be generally parallel to the lateral sides 65.
  • the ridges 60 may also travel parallel to or in angled directions from the anterior or posterior side 64, 66, without departing from the scope of the invention. While the ridges 60 are shown as linear, it will be appreciated that the ridges 60 may be non-linear without departing from the scope of the present invention.
  • the travel of the ridge 60 is generally along the entire length of the lateral side 65, but it may only travel a portion of the lateral side 65, or any side, without departing from the scope of the invention, and therefore is not limited to the length of travel that the ridge 60 makes along the second surface 34 of the endplate 11.
  • the endplate attachment screw 90 provides a locking mechanism for attachment of the endplate 11 to the inner core 15.
  • the first end 40 of the inner core 15 and the second end XX of the outer core 14 may consist of different configurations to attach the endplate 11 such as, by way of example, a sliding flange and groove method and a variable screw placement method.
  • the screw slot 63 allows for the insertion of an endplate attachment screw 90 to connect the endplate 11 to the inner core 15.
  • the endplate attachment screw 90 can hold the endplate to the inner core 15 by means of the screw slot flange 68 within the screw slot 63.
  • the endplates 11 may be generally oval or rectangular in shape (as shown in Figures 13-14) meaning they have a length dimension longer than a width dimension.
  • the endplates 11 may be circular in shape.
  • the different directions of travel of the ridges 60 on the second surface 34 cater to different spinal procedures, particularly pertaining to the direction of implant insertion.
  • an asymmetrical shape of endplate 11 is possible. This type of endplate is configured for a preferred use through a lateral approach, and generally under the
  • the width of an endplate is defined as the distance between the anterior side and posterior side of an endplate. Therefore, in one particular embodiment, the width of endplate 11 is preferably dimensioned generally in the range of 12-22mm.
  • the length of an endplate is defined as the distance between the opposing lateral sides of an endplate. Therefore, in one particular embodiment, the length of endplate 11 is preferably dimensioned generally in the range of 15-60mm.
  • the endplate 11 may also have a variety of shapes of the first and or second surfaces.
  • second surface 34 may be generally planar or the second surface 34 may be convexly curved to complement the contoured surface of a vertebral body endplate.
  • the endplate 11 may be provided with one of a variety of angles between the first surface 33 and second surface 34 of endplate 11.
  • Figure 16 demonstrates an exemplary embodiment of an angled endplate 94.
  • the angle 97 that will be described for endplate 94 is available in any of the previously described endplates and is therefore not limited to only endplate 94.
  • the angle 97 of the endplate 94 is preferably dimensioned generally in the range of -4 -15 degrees and functions to improve the natural curvature of the spine when implanted.
  • the preferred direction of the angle 97 formed between the first surface 33 and second surface 34 lies generally in a plane that is either along or parallel to a ridge 60, which in this example also happens to be parallel to the lateral sides 96. This configuration is intended to accompany specific procedures and directions that the endplate 94 will be implanted relative to adjacent vertebral bodies.
  • the angle 97 that is formed between the first surface 33 and second surface 34 may benefit the maintenance or correction of, for example, either the lordotic or kyphotic curvature of the spine, depending on the direction of angulation.
  • the distance between the first surface 33 and second surface 34 is greater at the anterior side 95 than the posterior side 98 of the endplate 94, then it can be assumed that the endplate 94 is configured to have the preferred use to correct or maintain lordosis.
  • One or more windows 30 provide for the insertion of bone growth material, blood and nutrient access throughout the area, and new bone growth to form around the implant.
  • Windows 30 can be of various shapes and sizes, and placed in different configurations on the second surface 34 in conjunction with the ridges 60 without departing from the scope of the present invention.
  • At least one marker rod 61 is press fit into the second side 34 of the endplate 11.
  • the shape of the marker rod 61 is generally conical.
  • the formation of the marker rods 46 are shown by example to be positioned in a rectangular formation, but can be positioned in other configurations without departing from the scope of the present invention.
  • any feature of the endplates disclosed herein by way of example only may be applied to any of the embodiments without departing from the scope of the present invention.
  • procedures described, for example only, involving specific regions of the spine e.g. thoracic and lumbar
  • may be applied to another region of the spine without departing from the scope of the present invention and dimensioning of the implant may be adjusted to accommodate any region.
  • Figures 17-27 illustrate examples of an expanding tool 200 for use with the vertebral body replacement implant assembly 10 described above.
  • the expanding tool 200 includes distal handle 201, outer cover 204, a proximal engagement region 202, adjustment region 203, and an elongated first shaft 144.
  • the proximal engagement region 202 includes a plurality of engagement arms 166, pusher arm 120 with pusher arm tip 161, locking pins 127, pushing spacer 160, extension piece 117 with engagement lip 18, one or more springs 125, slot pins 121, blocker bar 126, outer cover slots 122, and lower cover 156.
  • the adjustment region 203 includes large bezel 140, stopper rings 141, one or more holding rings 142, and a spur gear 142.
  • the outer cover 204 has a number of features that allow it to securely interface with vertebral body implant assembly 10, and specifically, the outer core 14.
  • the outer cover 204 consists of engagement arms 116 that are sized and dimensioned to securely slide into the indented slots 23 and secure the anti-rotation of the vertebral body implant assembly 10.
  • the fitting block 119 is sized and dimensioned to fit securely within the specially sized hole 88 in the outer core 14.
  • the distal handle 201 is connected to the elongated first shaft 110 such that the elongated first shaft 110 will rotate in conjunction with the rotation of the distal handle 201 due to the sleeve 211 and securing pin 212.
  • the outer cover 204 is connected to the distal handle 201 by the holding ring 142 that allows for the outer cover 204 to remain non-rotational.
  • the second shaft 144 will also not rotate with the rotation of the distal handle because the second shaft 144 is connected to the outer cover 204 (best seen in Figures 19 and 22).
  • the large bezel 140 is held in place by one or more stopping rings 141 and one or more holding rings 142.
  • a geared track 145 with teeth features 146 is inside of the large bezel 140 in which the spur gear 142 sits.
  • the spur gear teeth 147 interact with the teeth features 146 on the geared track 145 so that when the large bezel 140 is rotated, the spur gear rotates in the opposite direction.
  • Inner threads on the inside of the spur gear 142 match the threaded features 151 on the second shaft 144.
  • the inner threads interact with the threaded features 151 to transfer the rotational motion to axially motion and push the second shaft 144 horizontally parallel to the outer cover 204.
  • the spur gear 142 is kept in place by the stopper rings 141.
  • the second shaft 144 is held in place by the outer cover 204 and the lower cover 156.
  • Figure 19 shows adjustment region 203 with the large bezel 140 so that the inner workings can be appreciated.
  • the chief mechanisms for interface with the vertebral body implant assembly 10 are in the proximal engagement region 202.
  • the second shaft 144 is connected to the pushing spacer 160 by a locking pin 127.
  • the pushing spacer 160 is connected to the pusher arm 120 by another locking pin 127 that allows for horizontal movement of the pusher arm 120 when the pushing spacer 160 is moved closer to the engagement arms 116.
  • the spring 125 flexes so that the extension piece 117 will not move with the pusher arm 120.
  • the blocker bar 126 prevents the pusher arm 120 and extension piece 117 from moving vertically.
  • the slot pins 121 As the pusher arm 120 moves, the slot pins 121, specially designed to fit within the outer cover slots 122 (best seen in Figure 25), force the pusher arm 120 vertically upward because the slot pins 121 are traveling a prescribed path set by the outer cover slots 122.
  • the pusher arm tip 161 at the end of the pusher arm, acts on the extension piece 117 forcing it upward.
  • the extension piece 117 can be engaged when the outer cover 204 is in place with the engagement arms 116 securely in the indented slots 23 and the fitting block 119 resting in the specially sized hole 88. As described above, the rotation of the large bezel 140 pushes the extension piece 117 vertically upward where it can lock into the inside of the outer core 14 by the engagement lip 118. The engagement lip 118 ensures the outer core 14 will not move away from the expanding tool 200 when the expanding tool 200 is pushed up against the outer core 14 in order to rotate the adjustment ring 13.
  • the shaft end 130 sits inside the set screw opening 35 when the expanding tool 200 is properly connected to the vertebral body assembly 10.
  • the shaft end 130 includes adjustment features 131 that are sized and dimensioned to interact with external features 21 of the adjustment ring 13.
  • FIG. 26 and 27 show an alternative embodiment of the expanding tool 200.
  • the expanding tool 200 consists of a distal handle, outer cover 204, elongated first shaft 110, first shaft cover 209, second shaft 144, lover case cover 156, rotational gear 149, stopper rings 141, extension piece 117, and pusher arm 120.
  • the outer cover 204 includes a similar embodiment of the fitting block 119, discussed above, whereupon the fitting block 119 fits securely in the specially sized hole 88.
  • the shaft end 130 of the elongated first shaft 110 rests in the set screw opening 35.
  • the adjustment features 131 engage with the external features 21 of the adjustment ring 13.
  • the adjustment ring 13 then rotates changing the distance between the endplates 11.
  • This embodiment of the expanding tool 200 contains no mechanism to secure the vertebral body implant assembly 10 to the expanding tool 200.
  • FIG. 28A-28D illustrates one example of a preferred use of a vertebral body implant assembly 10 and the expanding tool 200.
  • Fig. 27A shows an anterior view of a portion of a spine, which includes a superior vertebra, a medial vertebra and an inferior vertebra which are shown labeled as VI, V2, and V3 respectively.
  • Fig. 27B the medial vertebra has been removed so that there is now a large space between the superior and inferior vertebral bodies.
  • endplates 11 have been chosen that are preferred for being positioned against the surfaces of the superior and inferior vertebral bodies. These selected endplates 11 are shown being attached to the inner core 15 and outer core 14 of the core expanding body 12.
  • the expanding tool 200 can then interface with the indented slots 23 of the outer core 14 by turning the distal handle 201.
  • the large bezel 140 is rotated to that the engagement lip 118 grasps the inside of the outer core 14 so that the core expanding body will not move when the distal handle 201 is rotated to change the axial distance between the endplates 11.
  • Figure 27C illustrates the vertebral body implant assembly 10 being inserted in its collapsed state from a lateral direction into the space remaining between the superior and inferior vertebral bodies using the expanding tool 200. While shown inserting from a lateral direction, the implant may also be inserted from an anterior approach, an anterior-lateral approach, a posterior approach or a posterior-lateral approach. To accommodate insertion from various approaches, the endplates 11 are coupled to the expandable body 12 in a position relative to the transverse axis of the expandable body 12 to facilitate the chosen approach. The height of the vertebral body implant assembly 10 is then increased by rotating the distal handle 201 which causes the adjustment ring 13 to rotate, as described above.
  • the adjustment features 131 of the shaft end 130 can engage the external features 21 of the adjustment ring 13 so that when the distal handle 201 and the elongated first shaft 144 rotate, the adjustment ring 13 rotates in concert.
  • rotation of the adjustment ring 13 causes expansion of the vertebral body implant assembly 10, as shown in Figure 27D.
  • the vertebral body implant assembly 10 is expanded until its desired height has been achieved. It is also possible to rotate the distal handle 201 in the opposite direction in order to cause the vertebral body implant assembly 10 to decrease in height.
  • the large bezel 140 is rotated in the direction to cause the retraction of the second shaft 144 and thereby the lowering of the extension piece 117 and engagement tip 118 to release the vertebral body implant assembly 10.
  • the expanding tool 200 is then separated from the vertebral body implant assembly 10 so that at least one set screw 16 from the outer core 14 can be engaged into the outer wall of the inner core 15 in order to secure the expanded height of the vertebral body implant assembly 10. Additional bone growth promoting material can then be added to the vertebral body implant assembly 10 before it is left to remain implanted between the first and second vertebrae.

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  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Neurology (AREA)
  • Transplantation (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Cardiology (AREA)
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  • Prostheses (AREA)

Abstract

La présente invention concerne un système et des procédés pour assembler et implanter un implant de corps vertébral. L'implant de corps vertébral comprend, mais n'est pas nécessairement limité à, un corps de noyau extensible et des plateaux qui peuvent être raccordés aux deux extrémités. Des plateaux de formes, tailles et angles divers peuvent être raccordés au noyau extensible dans une pluralité de positions de sorte qu'un implant de corps vertébral adapté puisse être implanté entre les vertèbres selon une approche antérieure, antéro-latérale, latérale, postérieure ou postéro-latérale.
PCT/US2012/050218 2009-03-12 2012-08-09 Remplacement de corps vertébral WO2013025448A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US14/177,100 US9687357B2 (en) 2009-03-12 2014-02-10 Vertebral body replacement
US15/635,087 US10390960B2 (en) 2009-03-12 2017-06-27 Vertebral body replacement
US16/510,123 US11458025B2 (en) 2009-03-12 2019-07-12 Vertebral body replacement
US17/822,877 US20220401228A1 (en) 2009-03-12 2022-08-29 Vertebral body replacement

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161521704P 2011-08-09 2011-08-09
US61/521,704 2011-08-09

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US12/661,206 Continuation-In-Part US9387090B2 (en) 2009-03-12 2010-03-12 Vertebral body replacement

Related Child Applications (1)

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US14/177,100 Continuation US9687357B2 (en) 2009-03-12 2014-02-10 Vertebral body replacement

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