Methods and Devices for Treating a Multi-Level Spinal Deformity
The present application discloses methods for treating a multi-level spinal deformity. The methods may include inserting a tether in a minimally-invasive manner through an entrance incision. The tether is moved along the spine and positioned to reduce and/or eliminate the deformity. Once the tether is positioned along the spine, the tether may be secured to the vertebral members. In one embodiment, the tether includes a rigid section and a flexible section. The tether may be positioned within the spine with the rigid section extending along a first length of the spine and the flexible section extending along a second length of the spine. The different sections provide different corrective forces to the spine to reduce and/or eliminate the spinal deformity. In one embodiment, the rigid section extends along an apex of the spinal deformity.
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The present application is directed to methods and devices for treating a multi-level spinal deformity and, more specifically, to a minimally-invasive method of inserting a tether into a patient.
The spine is divided into four regions comprising the cervical, thoracic, lumbar, and sacrococcygeal regions. The cervical region includes the top seven vertebral members identified as C1-C7. The thoracic region includes the next twelve vertebral members identified as T1-T12. The lumbar region includes five vertebral members L1-L5. The sacrococcygeal region includes nine fused vertebral members that form the sacrum and the coccyx. The vertebral members of the spine are aligned in a curved configuration that includes a cervical curve, thoracic curve, and lumbosacral curve.
Various deformities may affect the normal alignment and curvature of the vertebral members. Scoliosis is one example of a deformity of the spine in the coronal plane, in the form of an abnormal curvature. While a normal spine presents essentially a straight line in the coronal plane, a scoliotic spine can present various lateral curvatures in the coronal plane. The types of scoliotic deformities include thoracic, thoracolumbar, lumbar or can constitute a double curve in both the thoracic and lumbar regions. Schuermann's kyphosis is another example of a spinal deformity that affects the normal alignment of the vertebral members.
Tethers may be attached to the vertebral members to reduce and/or eliminate the deformity. However, it is often difficult to insert the tether into the patient without cutting tissue and/or muscle.
SUMMARYThe present application is directed to methods of inserting a tether into a body in a minimally-invasive manner. The methods may include creating an entrance incision for percutaneous insertion. A first end of the tether is moved into the entrance and the leads the remainder of the tether into the body. The tether may be moved along one or more fasteners that are attached to and extend outward from one or more vertebral members. Once the tether is positioned along the spine, the tether may be secured to the vertebral members.
In one embodiment, the tether includes a rigid section and a flexible section. The extent of the rigidity and flexibility may vary depending upon the context of use. The tether may be positioned within the spine with the rigid section extending along a first length of the spine and the flexible section extending along a second length of the spine. The different sections provide different corrective forces to the spine to reduce and/or eliminate the spinal deformity. In one embodiment, the rigid section extends along an apex of the spinal deformity.
The present application is directed to minimally-invasive methods of inserting a tether into a patient and attaching the tether to the vertebral members. The methods deliver a stabilizing means with minimal excision. The tether may be substantially flexible substantially along the entire length, or may include one or more rigid sections.
The tether 10 may be used for treating a variety of spinal deformities, including scoliosis.
In one embodiment, tether 10 is flexible along substantially the entire length. Embodiments include but are not limited to cables, artificial or synthetic strands, rods, plates, and springs. In one embodiment, tether 10 comprises an inner core with an outer sheath. The inner core and outer sheath may be made of a braided polymer such as polyester, polypropylene, or polyethylene. In one specific embodiment, the inner core and outer sheath are both made of polyethylene with the inner core being braided for strength and the outer sheath being braided for abrasion resistance. In one embodiment with the tether 10 being a strand, the strand may be manufactured from a variety of materials, including, but not limited to, conventional biocompatible implant alloys such as titanium, stainless steel, cobalt-chrome alloys, or even shape memory alloys and materials such as nickel-titanium.
In some embodiments, tether 10 includes one or more rigid sections 20 that are attached to one or more flexible sections 30. The sections 20, 30 may be attached together in a variety of manners. In some embodiments, a connector 21 is positioned between and connects the sections 20, 30.
Some embodiments feature the sections 20, 30 connecting directly together.
In some embodiments, tether 10 is a single member including sections with different physical properties.
Several methods of attaching together different elongated sections are disclosed in U.S. patent application Ser. No. 11/156,379 filed on Jun. 20, 2005 and entitled “Multi-Level Multi-Function Spinal Stabilization Systems and Methods” which is herein incorporated by reference.
The rigid section 20 includes a higher rigidity than the flexible section 30. In one embodiment, rigid section 20 includes a substantial strength to prevent bending, even during vertebral motion such as flexion, extension, and lateral bending. In one embodiment, rigid section 20 bends during vertebral motion. The rigid section 20 may be substantially straight, or may be curved to conform to the dimensions and shape of the vertebral members 90. The rigid section 20 may be constructed from a variety of different materials such as stainless steels, cobalt-chrome, titanium, and shape memory alloys. Non-metallic materials, including polymers made from materials such as PEEK and UHMWPE, are also contemplated.
Flexible section 30 includes a higher flexibility than the rigid section 20. Flexible section 30 may include a variety of different flexible materials including but not limited to cables, artificial or synthetic strands, rods, plates, and springs.
Various anchors 80 may be used to connect the tether 10 to the vertebral members 90.
Other anchors 80 may also be used for attaching the tether 10 to the vertebral members 90. In one embodiment, anchor 80 includes a fixed saddle 83 that does not move relative to the shaft 81. In another embodiment, anchor 80 is a staple that is substantially C-shaped to extend over and connect the tether 10 to the vertebral member 90.
The tether 10 is attached to the vertebral members 90 in a minimally-invasive manner. The tether 10 is fed through the skin, under the muscle, around the nerves, and over the vertebral members 90. Previous methods have disturbed the soft tissue and bone resulting in the body protecting the affected area by producing scar tissue and eventually fusing.
After the tether 10 is attached, the tool 300 is then manipulated by the surgeon to move the guide 200 and attached tether 10 through the fasteners 80. In one embodiment, the leading end 201 followed by the remainder of the guide 200 and the leading section of the tether 10 move through the saddle of the fastener 80. In one embodiment, the tool 300 is further inserted into the body 400 such that the leading end 201 is moved through the exit 201 and out of the body. The leading connector 209 is grasped by the surgeon at the exit 102 and the insertion tool 300 is disconnected from the tether 10 and removed from the body through the entrance 101.
In a similar embodiment, tether 10 includes a leading rigid section 20 and a flexible section 30. The rigid section 20 is attached directly to the insertion tool 30 and inserted into the body 400. In another embodiment, the tether 10 is inserted through the entrance 101 and positioned within the body 400 by the insertion tool 300. The insertion tool 300 is sized to move the tether 10 within the body 400 and does not require an exit incision 102.
The embodiment of
In one embodiment, a rigid section 20 is positioned at the apex of the spinal deformity. In another embodiment, a flexible section 30 is positioned at the apex of the spinal deformity.
In the various embodiments, the tether 10 may be inserted into the body 400 in either a cranial direction or a caudal direction.
The tether 10 may include one or more rigid sections 20 and one or more flexible sections 30. The lengths of each of the sections 20, 30 may be the same or may be different depending upon the context of use.
One embodiment includes accessing the spine from a postero-lateral, antero-lateral and lateral approaches to the spine. In another embodiment, the tether 10 is inserted with a posterior approach.
Spatially relative terms such as “under”, “below”, “lower”, “over”, “upper”, and the like, are used for ease of description to explain the positioning of one element relative to a second element. These terms are intended to encompass different orientations of the device in addition to different orientations than those depicted in the figures. Further, terms such as “first”, “second”, and the like, are also used to describe various elements, regions, sections, etc and are also not intended to be limiting. Like terms refer to like elements throughout the description.
As used herein, the terms “having”, “containing”, “including”, “comprising” and the like are open ended terms that indicate the presence of stated elements or features, but do not preclude additional elements or features. The articles “a”, “an” and “the” are intended to include the plural as well as the singular, unless the context clearly indicates otherwise.
The present invention may be carried out in other specific ways than those herein set forth without departing from the scope and essential characteristics of the invention. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive, and all changes coming within the meaning and equivalency range of the appended claims are intended to be embraced therein.
Claims
1-2. (canceled)
3. A method of treating a multi-level spinal deformity comprising:
- inserting a first end of a tether through an entrance incision into a body;
- threading the tether through a plurality of fasteners attached to vertebral members;
- positioning a rigid section of the tether at an apex of the spinal deformity;
- positioning a flexible section of the tether at an end of the rigid section
- moving the first end of the tether through an exit incision and out of the body; and
- securing the tether to each of the plurality of fasteners.
4-24. (canceled)
25. A method of treating a multi-level spinal deformity comprising:
- inserting a tether through an entrance incision;
- moving the tether through a plurality of fasteners each attached to one of a plurality of vertebral members;
- positioning a rigid section of the tether along a first section of the plurality of vertebral members;
- positioning a flexible section of the tether along a second section of the plurality of vertebral members;
- positioning a second rigid section of the tether along a third section of the plurality of vertebral members; and
- securing the tether to the plurality of vertebral members.
26-28. (canceled)
29. A method of treating a multi-level spinal deformity comprising:
- inserting a tether through an entrance incision;
- moving the tether along a plurality of vertebral members;
- positioning a rigid section of the tether along a first section of the plurality of vertebral members;
- positioning a flexible section of the tether along a second section of the plurality of vertebral members; and
- securing the tether to the plurality of vertebral members.
Type: Application
Filed: Aug 10, 2010
Publication Date: Dec 23, 2010
Applicant: WARSAW ORTHOPEDIC, INC. (Warsaw, IN)
Inventors: Randall Noel Allard (Issaquah, WA), Mark David Waugh (Germantown, TN), Larry Thomas McBride, JR. (Memphis, TN)
Application Number: 12/853,923
International Classification: A61B 17/88 (20060101);