US20140257403A1

US20140257403A1 - Methods for correcting spinal deformities

Info

Publication number: US20140257403A1
Application number: US14/283,931
Authority: US
Inventors: Fred J. Molz, IV
Original assignee: Warsaw Orthopedic Inc
Current assignee: Warsaw Orthopedic Inc
Priority date: 2006-09-14
Filing date: 2014-05-21
Publication date: 2014-09-11
Also published as: US9017388B2; US20080097433A1

Abstract

The present application is directed to devices and methods for correcting a spinal deformity. A spacer is positioned between processes that extend outward from a pair of vertebral members. A force applicator is operatively connected to apply a force to the vertebral members. The spacer then acts as a fulcrum with the force causing the vertebral members to pivot about the spacer and become aligned in a more desired orientation to eliminate or reduce the deformity.

Description

BACKGROUND

The present application is directed to methods for correcting spinal deformities and, more particularly, to methods that apply a corrective force to one or more of the vertebral members.
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. Intervertebral discs are positioned between the vertebral members and permit flexion, extension, lateral bending, and rotation.
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.

SUMMARY

The present application discloses methods for treating a spinal deformity. One method includes inserting a spacer between adjacent first and second vertebral members. A force applicator is then operatively connected to the vertebral members to apply a corrective force. The positioning of the spacer and the force applicator may vary depending upon the context of use. The applicator applies a force that causes the vertebral members to pivot about the spacer and become aligned to reduce the spinal deformity.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is schematic coronal view of a device positioned relative to a pair of vertebral members according to one embodiment.

FIG. 2 is schematic coronal view of an example of a scoliotic spine.

FIG. 3 is schematic sagittal view of a spacer and a force applicator mounted to vertebral members according to one embodiment.

FIG. 4 is a side view of a spacer according to one embodiment.

FIG. 5 is a side view of a spacer according to one embodiment.

FIG. 6 is side view of a spacer according to one embodiment.

FIG. 7 is perspective view of a spacer according to one embodiment.

FIG. 8 is a schematic sagittal view of spacers and tethers positioned relative to vertebral members according to one embodiment.

FIG. 9 is a schematic coronal view of spacers and tethers positioned relative to vertebral members according to one embodiment.

FIG. 10 is a schematic coronal view of a spacer and tether positioned relative to vertebral members according to one embodiment.

FIG. 11 is a schematic coronal view of a device positioned relative to a pair of vertebral members according to one embodiment.

DETAILED DESCRIPTION

The present application is directed to methods for correcting a spinal deformity. FIG. 1 illustrates a pair of vertebral members 90 and an intervertebral disc 91. A spacer 30 is positioned between processes 92 that extend outward from the vertebral members 90. A force applicator 40 is operatively connected to each of the vertebral members 90 to apply a compressive force as illustrated by arrows A to the vertebral members 90. The spacer 30 acts as a fulcrum with the compressive force causing the vertebral members 90 to pivot about the spacer 30. The spacer 30 also maintains the foraminal space while the force applicator 40 provides curve correction to eliminate or reduce the deformity.
FIG. 2 illustrates a patient's spine that includes a portion of the thoracic region T, the lumbar region L, and the sacrum S. This spine has a scoliotic curve with an apex of the curve being offset a distance X from its correct alignment in the coronal plane. The spine is deformed laterally so that the axes of the vertebral members 90 are displaced from the sagittal plane passing through a centerline of the patient. In the area of the lateral deformity, each of the vertebral members 90 includes a concave side 90 a and a convex side 90 b. One embodiment of the devices and methods position a fulcrum 30 on the convex side 90 b of two or more adjacent vertebral members 90. A compressive force is applied to the convex side 90 b of the vertebral members 90 to reduce and/or eliminate the spinal deformity. In one embodiment, a distractive force is applied to the concave side 90 a to reduce and/or eliminate the spinal deformity.
FIG. 3 illustrates one embodiment that corrects the spinal deformity. A spacer 30 is positioned between the spinous processes 92 a that extend outward from the posterior of each of the vertebral members 90. The force applicator 40 is attached to the convex side 90 b of the vertebral members 90. The force applicator 40 applies a corrective force to the vertebral members 90 to provide curve correction. Spacer 30 is used as a fulcrum for the vertebral members 90 and also maintains the foraminal space. The spacer 30 and force applicator 40 may be effective in patients with remaining skeletal growth.
Spacer 30 also acts as a positioning device to reduce the load placed onto specific areas of the vertebral members 90. Prior art methods have included tethering that place an abnormally large load on the facet joints. This may cause the facet joints to experience excessive wear resulting in damage to the vertebral members 90, and/or pain to the patient. Spacer 30 absorbs all or a part of the load to reduce and/or eliminate wear on the facet joints and pain to the patient.
Spacer 30 may include a variety of shapes and sizes. FIG. 4 illustrates an embodiment with a central section 34 with superior and inferior arms 32 that are spaced apart with a gap 33 formed therebetween. The spacer 30 is positioned with the processes 92 positioned within each of the gaps 33 and being separated by the central section 34. The arms 32 extend along the lateral sides of each of the processes 92 to maintain the attachment. FIG. 5 illustrates another embodiment of a spacer 30 with enlarged lateral end sections 36 forming inferior and superior indents 37 to receive the spinous processes 92 a. The central section 34 formed between the indents 37 separates the spinous processes 92 a. FIG. 6 illustrates an embodiment with a central section 34 sized to space the spinous processes 92 a. FIG. 7 includes an offset central section 34 with inferior and superior arms 32 positioned to contact the spinous processes 92 a.
The spacer 30 may be formed for a variety of biocompatible polymeric materials, including elastic materials, such as plastics, metals, elastomeric materials, hydrogels or other hydrophilic-polymers, or composites thereof. The nature of the materials employed to form the spacer 30 may be selected to exhibit a sufficient stiffness to space apart the spinous processes 92 a. The term stiffness is used to refer to the resistance of an elastic body to deflection by an applied force.
The spacer 30 may also be fully or partially constructed from bio-absorbable material. Bio-absorbable material provides the positioning and/or stiffness functions for a limited time after the spacer 30 is implanted and is then eventually absorbed by the body. In one embodiment, the bio-absorbable material is gradually absorbed by the body. During this initial period, the body may heal to an extent that the spacer 30 is adequate to support the vertebral members 90 and/or the body is able to position the spacer 30. In one embodiment, the bio-absorbable material is replaced with tissue, such as fibrous tissue and fibrous scar tissue. The bio-absorbable material may be formed from a wide variety of natural or synthetic materials including fibrin, albumin, collagen, elastin, silk and other proteins, polyethylene oxide, cyanoacrylate, polylactic acid, polyester, polyglycolic acid, polypropylene fumarate, tyrosine-based polycarbonate and combinations thereof. Other suitable materials include demineralized bone matrix. In one embodiment, bio-absorbable material may be a woven fabric.
Various embodiments of spacers 30 are disclosed in U.S. patent application Ser. Nos. 11/341,233 and 11/341,200 each filed Jan. 27, 2006 and each entitled “Interspinous Devices and Methods of Use”. These applications are hereby incorporated by reference. Another embodiment of a spacer is the DIAM Spinal Stabilization System available from Medtronic Sofamor Danek of Memphis, Tenn., also hereby incorporated by reference.
In one embodiment, the force applicator 40 applies a compressive force to the convex side 90 b of the vertebral members 90. FIG. 3 illustrates one embodiment of the force applicator 40 that includes an anchor 41 mounted within each of the vertebral members 90. A tether 42 extends between and is operatively connected to each anchor 41. Anchors 41 include a shaft that mounts within the vertebral member, and a head that extends outward beyond the vertebral member 90. The anchors 41 can be made from a variety of biocompatible materials, including synthetic or natural autograft, allograft or xenograft tissues, and can be resorbable or non-resorbable nature. Examples of tissue materials include hard tissues, connective tissues, demineralized bone matrix and combinations thereof. Further examples of resorbable materials are polylactide, polyglycolide, tyrosine-derived polycarbonate, polyanhydride, polyorthoester, polyphosphazene, calcium phosphate, hydroxyapatite, bioactive glass, and combinations thereof. Further examples of non-resorbable materials are carbon-reinforced polymer composites, shape-memory alloys, titanium, titanium alloys, cobalt chrome alloys, stainless steel, ceramics and combinations thereof. Each of the anchors 41 may be substantially the same, or different in both size, shape, and materials.
Various types of tethers 42 may be used to apply the force. FIG. 3 illustrates a rod that connects with and extends between the anchors 41. A first end of the rod is connected to the superior anchor 41, and a second end is connected to the inferior anchor 41. FIG. 8 illustrates another embodiment with cables 42 that extend between the anchors 41. Other embodiments may include, but are not limited to, staples, cables, artificial strands, rods, plates, springs, artificial ligaments, and combinations thereof. The tethers 42 may be rigid, semi-rigid, flexible, partially flexible, resorbable, non-resorbable, superelastic, or include shape-memory material. Further examples of tether constructs include those that are single strand, multiple strands, braided, or combinations thereof.
In some embodiments, the tether 42 is constrained to the anchors 41. Other embodiments may include the tether 42 being unconstrained or semi-constrained connections. Still other embodiments may include connections that are combinations of the above. An example of a semi-constrained connection is a ball joint that allows at least some range of articulation of the construct relative to the anchor, or float within a neutral zone. Examples of constrained or semi-constrained connections include a construct that is wrapped around, crimped, clamped or penetrated by a portion of the anchor or a set screw or cap engageable to the anchor. Such constrained connections fix the construct to the anchor so that there is no or minimal relative movement therebetween
Tether material can include but is not limited to polymers, such as polyester and polyethylene; superelastic metals, such as nitinol; shape memory alloy, such as nickel titanium; resorbable synthetic materials, such as suture material, metals, such as stainless steel and titanium; synthetic materials, allograft material; and bioelastomer material. U.S. Patent Application Publication 2003/0088251 discloses various types of anchors and tethers and is herein incorporated by reference.
The spacer 30 may be positioned at different locations relative to the vertebral members 90. In the embodiment of FIG. 3, spacer 30 is positioned between the spinous processes 92 a. In another embodiment, the spacer 30 is positioned between the transverse processes 96 as illustrated in FIG. 8. FIG. 8 specifically illustrates an embodiment with two separate spacers 30 a, 30 b positioned between the transverse processes 96 a, 96 b, 96 c of three separate vertebral members 90. In another embodiment (not illustrated), a first spacer is positioned between the transverse processes, and a second spacer is positioned between the spinous processes.
FIG. 11 illustrates another embodiment with the spacer 30 attached to the vertebral members 90 with anchors 41. A first surface of the spacer 30 is placed against the vertebral members 90 with a second surface facing outward. One or more anchors 41 may attach the spacer 30 to each vertebral member 90. The force applicator 40 applies a force to the vertebral members 90 causing them to pivot about the spacer 30. This positioning allows for the spacer 30 to act as a fulcrum at other positions than between the spinous processes 92 and transverse processes 96.
Some embodiments include a single spacer 30. This usually occurs when the tether 42 extends between two adjacent vertebral members 90. FIG. 3 illustrates an example of a single spacer 30. Other embodiments feature multiple spacers 30 such as FIG. 8. Multiple spacers 30 may be required when a tether 42 or combination of tethers 42 extends to three or more vertebral members 90. In some embodiments, two or more force applicators 40 are attached to the vertebral members 90.
In the embodiment illustrated in FIG. 3, the force applicator 40 is attached to the convex side 90 b of the vertebral members 90. The force applicator 40 applies a compressive force to the convex side 90 b to arrest or at least minimize growth on the convex or “long” side 90 b of the spine, thereby allowing the concave or “short” side 90 a of the spine to grow and catch up with the long side. In another embodiment, force applicator 40 is attached to the concave side 90 a and applies a distractive force to the vertebral members 90. This distractive force causes the vertebral members 30 to move about the spacer 30. In distractive force applications, the spacer 30 may be positioned on an opposite side of the vertebral member 90 from the force applicator 40. By way of example, a spacer 30 is positioned on the convex side 90 b when a force applicator 40 is attached to and applies a distractive force to the concave side 90 a.
In one embodiment, a single force applicator 40 and spacer 30 are attached to a single level of the spine, such as at the apex of the deformity. Using FIG. 2 as an example, the force applicator 40 and spacer 30 may span between the T9-T10 vertebral members 90. Alternatively, additional applicators 40 and/or spacers 30 may further span to the adjacent vertebral members 90 which in this example include T8 and T11. In other embodiments, force applicators 40 and spacers 30 may be used at multiple levels of the spine. By way of example, a first applicator 40 and spacer 30 may span between T10-T11, with a second applicator 40 and spacer 30 spanning T12-L1.
It should be understood that the spinal deformity depicted in FIG. 2 is but one of many types of spinal deformities that can be addressed by the devices and techniques of the present application. Most commonly the devices and methods are expected to be used for either primary thoracic or thoracolumbar curves. They can be used for correction of the thoracic curve as an isolated curve, or the lumbar curve as an isolated curve. The devices may further be used in combination with the shortening of the opposite side of the vertebral member 90.
The devices and methods may be used to treat spinal deformities in the coronal plane, such as a scoliotic spine illustrated in FIG. 2. The devices and methods may also be used to treat deformities in the sagittal plane, such as a kyphotic spine or Scheurmann's kyphosis. FIGS. 9 and 10 illustrate embodiments for treating such deformities. One or more tethers 42 are attached to a posterior section of the vertebral members 90. The tethers 42 may extend across two or more of the vertebral members 90 depending upon the context of use. One or more spacers 30 are positioned between the vertebral members 90. In some embodiments, spacers 30 are positioned between the transverse processes 98. The spacer or spacers 30 may relieve some of the force applied to the facet joints. In addition, a spacer 30 may be positioned between the spinous processes 92 (not illustrated). In another embodiment, one or more tethers 42 are positioned on the posterior of the vertebral members 90 without use of a spacer 30.
One embodiment includes accessing the spine from an anterior approach. Other applications contemplate other approaches, including posterior, postero-lateral, antero-lateral and lateral approaches to the spine, and accessing various regions of the spine, including the cervical, thoracic, lumbar and/or sacral regions.
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 force applicator 40 may apply a force to arrest or minimize growth of the convex side 90 b of the vertebral members 90, or alternatively, to simply prevent further deformity of the spine. 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

1-30. (canceled)

31. A method for treating a spinal deformity, comprising the steps of:

distracting adjacent vertebral bodies; and

compressing the adjacent vertebral bodies.

32. A method as recited in claim 31, wherein the step of distracting the adjacent vertebral bodies comprises applying a distraction force by inserting a spacer between the adjacent vertebral bodies.

33. A method as recited in claim 32, further comprising pivoting the adjacent vertebral bodies and deforming the spacer.

34. A method as recited in claim 31, wherein the step of distracting the adjacent vertebral bodies comprises applying a distraction force by inserting a spacer between the adjacent vertebral bodies such that the spacer engages a transverse process of each of the adjacent vertebral bodies.

35. A method as recited in claim 31, wherein the step of compressing the adjacent vertebral bodies comprises applying a compression force by attaching a force applicator to an exterior of each of the adjacent vertebral bodies.

36. A method as recited in claim 35, wherein the exterior of each of the adjacent vertebral bodies is a posterior section of each of the adjacent vertebral bodies.

37. A method as recited in claim 35, wherein the step of attaching the force applicator to the exterior of each of the adjacent vertebral bodies comprises mounting an anchor in the exterior of each of the adjacent vertebral bodies, the force applicator being constrained to the anchors.

38. A method as recited in claim 37, wherein at least one of the anchors is resorbable.

39. A method as recited in claim 31, wherein:

the step of distracting the adjacent vertebral bodies comprises applying a distraction force by inserting a spacer between the adjacent vertebral bodies such that the spacer engages a transverse process of each of the adjacent vertebral bodies;

the step of compressing the adjacent vertebral bodies comprises applying a compression force by attaching a force applicator to an exterior of each of the adjacent vertebral bodies.

40. A method as recited in claim 39, wherein the step of distracting the adjacent vertebral bodies occurs at the same time as the step of compressing the adjacent vertebral bodies.

41. A method as recited in claim 39, wherein:

the compression force causes the adjacent vertebral bodies to move about the spacer and treat the spinal deformity; and

moving the adjacent vertebral bodies about the spacer causes the adjacent vertebral bodies to pivot and deform the spacer.

42. A method as recited in claim 39, wherein the compression force is applied to the transverse processes.

43. A method for treating a spinal deformity, comprising the steps of:

distracting adjacent vertebral bodies; and

compressing the adjacent vertebral bodies,

wherein the step of distracting the adjacent vertebral bodies occurs at the same time as the step of compressing the adjacent vertebral bodies.

44. A method as recited in claim 43, wherein:

the step of compressing the adjacent vertebral bodies comprises applying a compression force by attaching a force applicator to an exterior of each of the adjacent vertebral bodies; and

the force applicator is spaced apart from the spacer.

45. A method as recited in claim 44, further comprising pivoting the adjacent vertebral bodies and deforming the spacer.

46. A method as recited in claim 44, wherein the compression force causes the adjacent vertebral bodies to move about the spacer and treat the spinal deformity.

47. A method for treating a spinal deformity, comprising the steps of:

distracting adjacent vertebral bodies by application of a distraction force between processes of adjacent vertebral bodies; and

compressing the adjacent vertebral bodies by application of a compression force on the processes of the adjacent vertebral bodies.

48. A method as recited in claim 47, wherein the processes of the adjacent vertebral bodies are transverse processes.

49. A method as recited in claim 47, wherein:

the distraction force is created by inserting a spacer between the adjacent vertebral bodies such that the a transverse process of each of the adjacent vertebral bodies is disposed in a gap defined by arms of the spacer; and

the compression force is created by attaching a force applicator to an exterior of a posterior section of each of the adjacent vertebral bodies by mounting an anchor into the exterior of each of the adjacent vertebral bodies.

50. A method as recited in claim 49, wherein:

the step of distracting the adjacent vertebral bodies occurs at the same time as the step of compressing the adjacent vertebral bodies;