This invention relates to the insertion of one or more spacing means in the human vertebral column and is an improved means of provision and insertion off such spacing means. Recent advances in minimally invasive spinal surgery have led to the adoption of spacing means in order to increase the distance between adjacent spinous processes extending from the rear of the spinal vertebrae. Such spacing means are presently marketed by U.S. companies such as Medtronics Inc. and Saint Francis Medical Inc. and details of such means are show in the attached documents B1 and B2 which are copies of the brochures of the above mentioned companies relating to these products.
The present spacing means each suffer a distinct disadvantage in that due to their size and other considerations neither of them is suitable for use in the cervical spine. Further the said spacing means each require the creation of a significant surgical trauma in order to provide access for the insertion of the said spacing means into the human body. It is an object of the present invention to provide a spacing means which can be positioned between the spinous processes using only a minimally invasive surgical procedure thereby reducing the degree of trauma suffered by the patient and hence the time required for the healing of the insertion wound.
The present invention is described by reference to
The first portion (8) of the said first embodiment, of the device is comprised of one or more components, which singly or together form a section of a tapered screw the root of which (10) may be advantageously disposed more or less parallel to the longitudinal axis of the device and which may be of a form (not shown) appropriate for the location of one or more spinous processes which may rest on the said root.
The second portion (9) of the said first embodiment of the device comprises a spacing member which will be inserted between the said processes of the said spinal vertebrae during the required surgical procedure and which will remain in position upon the completion of the surgical procedure. The said second portion comprises a central hub (11) of a form which is adapted so as to provide a surface upon which the said spinous processes may bear when the said second portion rests between two such spinous processes. The cross-sectional profile of the said hub, which lies at right angles to the horizontal axis through the center of the component may vary along the direction of the said horizontal axis so as to provide lateral location for the spinous processes, which rest against it (not shown).
As can be seen in
In order to effect the insertion of the spacing member (9) the surgeon first provides access to the left and right hand sides of the adjacent spinous processes between which it is desired to insert the said spacing member using minimally invasive techniques known to those skilled in the surgical art. The assembled first embodiment of the device is inserted into the area between the adjacent spinous processes and rotated using a driving tool (not shown) which may be advantageously fitted with a ratchet device for ease of operation. As the said first embodiment of the device advances through the space between the adjacent spinous processes the increasing cross-sectional dimensions of the root of the first portion of the device causes the adjacent spinous processes to progressively separate.
The said second component (9) of the first embodiment of the device is selected by the surgeon to provide the desired spacing between the adjacent spinous processes upon completion of the surgical procedure. When the said second component of the device enters the space between the adjacent spinous processes and has been set at the appropriate rotational angle, the leading end of the first portion of the screw-like device may be accessed on the left-hand side of the spinous processes. The shaped nut (6) which has been screwed on to the shaped rod (2) during the assembly of the device may now be gripped using a surgical pliers and rotated so as to remove it from the screwed end of the shaped rod. Alternatively the shaped nut (6) may be provided with a means of attaching a special-purpose tool (not shown) which may in turn be provided with a ratchet for ease of operation in removing the shaped nut from the said shaped rod.
Following the removal of the shaped nut (6) from the shaped rod (2), the shaped rod is withdrawn by the surgeon from the right hand side of the spinous processes. At this point, a second shaped rod (not shown) having cross-sectional dimensions similar to those of the said square section hole (7a) in the said first component of the first embodiment of the device, but smaller than those of the square section hole (7b) in the said second component (9) of the device (alternatively referred to as “the spacing member”) is inserted from the right hand side of the spinous processes and fed through the larger square hole (7b) in the said spacing member (9) so as to pass through the smaller square section hole (7a) in the said first component of the first embodiment of the device. The shaped nut (6) is now screwed onto the threaded end of the said second shaped rod and the first component (8) of the device is now rotated by means of the smaller shaped rod so as to drive it forward, releasing it from the patient's body to the left of the spinous processes. The said shaped nut (6) is now unscrewed from the said second shaped rod and the rod is withdrawn from the body of the patient on the right hand side of the spinous processes leaving the said second component (or spacing member) (9) of the said segmented tapered screw assembly disposed between the spinous processes of the required adjacent vertebrae. In performing the surgical procedure the insertion of the spacing member may, if desired, be made from the left hand side of the spinous processes in which event the instructions as to left hand and right hand positioning are interchanged. The spacing member (9) may, if desired, be provided with an attached clip or suture (not shown) by means of which it may be secured to the adjacent spinous processes in order to prevent dislodgement.
In a second and preferred embodiment of the device shown in
The assembled device is inserted using a shaped rod the end portion of which is shown at (18 in
In a further embodiment shown in
The device of the invention may be fabricated from any material, which is suitable for use in the human body. The preferred material for first and second components as well as the blind nut may be any plastic material, which has been formulated for use in the human body. The said plastic material may be coated or treated with other material in order to render it more compatible with surrounding tissue. The spring clips referred to in relation to second and third embodiments may be advantageously formed from stainless spring steel or any suitable metal alloy.
In order to facilitate viewing of the device during insertion in the human body, the material of the said flexible enclosure may be rendered radio-opaque by inclusion therein of a radio opaque material in forms familiar to those skilled in the art of radiographic imaging.
The device of the invention may be manufactured in a variety of sizes suitable for insertion at different points in the spinal column. First and second components of different sizes may be combined to achieve the best result in any given location. The device of the invention has the advantage of entitling the necessary independent displacement of the adjacent vertebrae to the required separation, which is achieved automatically upon the positioning of the spacing member of the device between the adjacent spinous processes. It is thus unnecessary to increase the separation of the adjacent vertebrae beyond the desired separation in order to facilitate the insertion of the spacing member.
Number | Date | Country | Kind |
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0605962.0 | Mar 2006 | GB | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US07/07243 | 3/23/2007 | WO | 00 | 4/20/2010 |