1. Technical Field
The present disclosure relates to devices, systems and methods for spinal stabilization. More particularly, the present disclosure relates to devices, systems and methods for providing dynamic stabilization to the spine via the use of elongated members spanning one or more spinal levels.
2. Background Art
Each year, over 200,000 patients undergo lumbar fusion surgery in the United States. While fusion is a well-established procedure that is effective about seventy percent of the time, there are consequences even to successful fusion procedures, including a reduced range of motion and an increased load transfer to adjacent levels of the spine, which may accelerate degeneration at those levels. Further, a significant number of back-pain patients, estimated to exceed seven million in the U.S., simply endure chronic low-back pain, rather than risk procedures that may not be appropriate or effective in alleviating their symptoms.
New treatment modalities, collectively called motion preservation devices, are currently being developed to address these limitations. Some promising therapies are in the form of nucleus, disc or facet replacements. Other motion preservation devices provide dynamic internal stabilization of the injured and/or degenerated spine, e.g., the Dynesis stabilization system (Zimmer, Inc.; Warsaw, Ind.) and the Graf Ligament. A major goal of this concept is the stabilization of the spine to prevent pain while preserving near normal spinal function.
In general, while great strides are currently being made in the development of motion preservation devices, the use of such devices is not yet widespread. One reason that this is so is the experimental nature of most such devices. For example, to the extent that a given motion preservation device diverges, whether structurally or in its method of use or implementation, from well-established existing procedures such as lumbar fusion surgery, considerable experimentation and/or testing is often necessary before such a device is given official approval by governmental regulators, and/or is accepted by the medical community as a safe and efficacious surgical option.
With the foregoing in mind, those skilled in the art will understand that a need exists for spinal stabilization devices, systems and methods that preserve spinal motion while at the same time exhibiting sufficient similarity to well-established existing spinal stabilization devices, systems and methods so as encourage quick adoption/approval of the new technology. These and other needs are satisfied by the disclosed devices, systems and methods that include elongated members for implantation across one or more levels of the spine.
According to the present disclosure, advantageous devices, systems, kits for assembly, and/or methods for dynamic stabilization are provided. According to exemplary embodiments of the present disclosure, the disclosed devices, systems, kits and methods include an elongated member, e.g., a spinal support rod, that is configured and dimensioned for implantation adjacent the spine of a patient so as to promote efficacious spinal stabilization. The disclosed elongated member extends axially, e.g., as do spinal support rods used in connection with lumbar fusion and other related procedures. Among other similarities therewith, e.g., such as are described hereinbelow, the disclosed elongated member is substantially dimensionally stable, both radially and axially. Among some differences therewith, e.g., such as are described below, the disclosed elongate member is capable of bending, flexing, and/or deflecting laterally (e.g., along any and/or substantially all transverse directions) to an extent that preserves a degree of spinal motion.
According to exemplary embodiments of the present disclosure, the elongated member includes an axial span that extends in an axial direction across a spinal level to promote efficacious spinal stabilization thereacross, and that manifests a radially segmented geometry relative to the axial direction. In some such embodiments, the elongated member is configured and dimensioned for implantation adjacent the spine such that at least two axial spans of the elongated member extend across respective spinal levels of the spine to promote efficacious spinal stabilization across both such spinal levels. In some such embodiments, the axial span has a rod-like profile and is adapted to be coupled to the spine of the patient via attachment to conventional spine attachment devices configured for coupling conventional support rods, such as solid, relatively inflexible spinal support rods used in conjunction with spinal fusion assemblies, to the spine. In alternative embodiments of the present disclosure, the axial span is adapted to be mounted with respect to a patient's spine using alternative mounting structures/members, e.g., mounting hooks, plates, cemented stems, or the like. Such rod-like profile can include a diameter in a range of from about 5.5 mm to 6.35 mm (although alternative dimensions are contemplated), and the axial span can be adapted to permit pedicle screws to be attached to the elongated member at multiple points along the length of the axial span so as to accommodate a range of different patient anatomies and intervertebral heights. Further with respect to some such exemplary embodiments, the axial span is axially substantially rigid as against axial forces arrayed in compression and/or tension.
Still further with respect to some such exemplary embodiments, the radially segmented geometry manifested by the axial span permits the axial span to bend, flex or deflect along any and substantially all transverse directions while providing efficacious spinal stabilization across the spinal level during at least one of spinal flexion, spinal extension, spinal lateral bending, and spinal axial rotation. According to exemplary embodiments, the axial span provides efficacious spinal stabilization across the spinal level during: a) spinal flexion in which the spinal level defines an anterior bend of at least approximately five to seven degrees; b) spinal extension in which the spinal level defines a posterior bend of at least approximately three to seven degrees; and/or c) spinal bending in which said spinal level defines a lateral bend of at least approximately four to seven degrees. Yet further with respect to some such embodiments, the radially segmented geometry includes a rod of radially unitary construction and extending in the axial direction, and at least one sleeve extending in the axial direction and surrounding the rod. According to further exemplary embodiments, the rod can be fabricated, in whole or in part, from a superelastic material.
According to further embodiments of the present disclosure, a surgically implantable spinal support rod is provided that includes an axial span that extends in an axial direction so as to span at least one spinal level, wherein the axial span manifests (at least in part) a radially segmented geometry relative to the axial direction. In some such embodiments, the radially segmented geometry manifested by the axial span includes at least one pair of axially-extending adjacent surfaces adapted to move relative to each other along the axial direction during a transverse deflection of the axial span. Such at least one pair of axially-extending adjacent surfaces can include first and second substantially cylindrically shaped surfaces, wherein each such surface faces radially outerward toward the other such surface, or wherein such surfaces are substantially aligned with respect to each other. In others of such embodiments, the axial span has a rod-like profile, and is adapted to be coupled to the spine of the patient via attachment to conventional spine attachment devices configured for coupling conventional support rods to the spine for purposes of spinal fusion. Such rod-like profile of the axial span can include a diameter in a range of from about 5.5 mm to 6.35 mm, although alternative dimensions and/or dimensional ranges may be employed.
In accordance with still further embodiments of the present disclosure, a kit for assembling a dynamic spinal support system is provided. Such kit includes a spinal support rod having an axial span extending in an axial direction so as to span at least one spinal level, and manifesting a radially segmented geometry relative to said axial direction. Such kit also includes a plurality of spine attachment devices attachable to the axial span so as to couple the spinal support rod to the spine of the patient across the spinal level. In some such embodiments, at least one of such spine attachment devices includes a pedicle screw, hook, plate and/or cemented stem.
In accordance with another embodiment of the present disclosure, the elongated member includes an axial span that extends in an axial direction across at least one spinal level to promote efficacious spinal stabilization thereacross, and that includes a sleeve and a series of structural members aligned along the axial direction, enclosed within the sleeve, and adapted to support the sleeve against lateral buckling, e.g., when the sleeve experiences a lateral bend and is supporting the spine across the at least one spinal level. In some such embodiments, the sleeve is adapted to generate an internal spring force in opposition to the lateral bend as the sleeve deflects so as to accommodate and moderate the lateral bend. In exemplary embodiments, the sleeve can be fabricated, at least in part, from a superelastic material, such as an alloy of nickel titanium. The structural members can be substantially spherical in shape and, in such embodiments, the sleeve can be substantially cylindrical in shape.
In accordance with yet another embodiment of the present disclosure, the elongated member includes an axial span that extends in an axial direction across at least one spinal level to promote efficacious spinal stabilization thereacross, and further includes an axial sleeve and a coil spring disposed within the axial sleeve. In some such embodiments, the sleeve is fabricated from a superelastic material and/or an alloy of titanium. In some other such embodiments, the sleeve is fabricated from a polymeric material. In some other such embodiments, the coil spring is sized and oriented so as to support a peripheral shape of the axial sleeve against at least one of crushing and buckling during spinal stabilization.
In accordance with another embodiment of the present disclosure, the elongated member includes an axial span that extends in an axial direction across at least one spinal level to promote efficacious spinal stabilization thereacross, and further includes an axially-extending coil spring and a restraining element disposed within the coil spring and extending at least partially through the coil spring in the axial direction so as to limit an axial extension of the elongated member. In some such embodiments, the restraining element includes a cable adapted to render the elongated member substantially rigid as against axial forces arrayed in compression. The cable can take the form of a wire rope cable.
According to further embodiments of the present disclosure, a surgically implantable spinal support rod is provided that includes an axial span that extends in an axial direction so as to span at least one spinal level, wherein the disclosed spinal support bar is of unitary construction, both along the axial direction, and radially relative to the axial direction, and is further adapted to deflect laterally so as to permit at least three to seven degrees of bending in the spine across the at least one spinal level in at least one of spinal flexion, spinal extension, and spinal lateral bending. In some such embodiments, the spinal support bar manifests a substantially constant cross-sectional geometry across the at least one spinal level, e.g., a circular cross-sectional geometry. In some other such embodiments, the spinal support bar includes a central span extending in the axial direction, and channels formed in the central span so as to increase transverse flexibility of the central span. Such channels can extend in the axial direction, and/or such channels can extend transversely relative to the axial direction. In some other such embodiments, the spinal support bar includes a central span, a first end span, and a second end span disposed opposite the central span from the first end span. The central span may be associated with a reduced cross-sectional area relative to respective cross-sections of the first and second end spans, e.g., the central span can be associated with a circular cross section of a reduced diameter relative to respective circular cross-sections of the first and second end spans.
The elongated members/spinal support rods of the present disclosure, and/or the spinal stabilization devices/systems of the present disclosure incorporating such elongated members/spinal support rods, advantageously include one or more of the following structural and/or functional attributes:
Advantageous spine stabilization devices, systems, kits for assembling such devices or systems, and methods may incorporate one or more of the foregoing structural or functional attributes. Thus, it is contemplated that a system, device, kit and/or method may utilize only one of the advantageous structures/functions set forth above, or all of the foregoing structures/functions, without departing from the spirit or scope of the present disclosure. Stated differently, each of the structures and functions described herein is believed to offer benefits, e.g., clinical advantages to clinicians or patients, whether used alone or in combination with others of the disclosed structures/functions.
Additional advantageous features and functions associated with the devices, systems, kits and methods of the present disclosure will be apparent to persons skilled in the art from the detailed description which follows, particularly when read in conjunction with the figures appended hereto. Such additional features and functions, including the structural and mechanistic characteristics associated therewith, are expressly encompassed within the scope of the present invention.
To assist those of ordinary skill in the art in making and using the disclosed devices and systems, reference is made to the appended figures, in which:
The present disclosure provides advantageous devices, systems and methods for providing dynamic spinal stabilization. More particularly, the present disclosure provides elongated members in the form of rods that are suitable for surgical implantation across multiple spinal levels for purposes of support and stabilization in flexion, extension and/or axial rotation, and that are also laterally flexible so as to provide a range of motion in spinal flexion, extension and/or axial rotation.
The exemplary embodiments disclosed herein are illustrative of the advantageous spinal stabilization devices/systems and surgical implants of the present disclosure, and of methods/techniques for implementation thereof It should be understood, however, that the disclosed embodiments are merely exemplary of the present invention, which may be embodied in various forms. Therefore, the details disclosed herein with reference to exemplary dynamic stabilization systems and associated methods/techniques of assembly and use are not to be interpreted as limiting, but merely as the basis for teaching one skilled in the art how to make and use the advantageous spinal stabilization systems and alternative surgical implants of the present disclosure.
With reference to
Each of the spine attachment elements 12, 14, 16 of the spinal stabilization system 10 includes an attachment extension 20 (depicted at least partially schematically) and an attachment member 22 (also depicted at least partially schematically). The spine attachment elements 12, 14, 16 are securely affixed to the respective vertebrae V1, V2, V3 via respective ends of the attachment extensions 20 being embedded within corresponding voids in the tissue of the respective vertebrae V1, V2, V2, and being securely retained therein (i.e., so as to prevent the attachment extensions 20 from being pulled out of their respective voids, or rotated with respect thereto, whether axially or otherwise). The attachment extensions 20 are embedded into and/or retained within their respective vertebral voids via suitable conventional means, such as a helical thread and/or a helically-shaped inclined plane formed on the respective attachment extension 20, a biocompatible adhesive, or other means of embedding and/or retention. The attachment extensions 20 form respective parts of and/or are mounted with respect to respective pedicle screws of conventional structure and function in accordance with at least some embodiments of the present disclosure. The attachment extensions 20 form parts of other types of structures than that of conventional pedicle screws in accordance with some other embodiments of the present disclosure, e.g., hooks, plates, stems or the like.
The attachment extensions 20 and attachment members 22 of the spine attachment elements 12, 14, 16 are attached or coupled with respect to each other at respective ends of the attachment extensions 20 opposite the ends thereof that are embedded within the tissue of the respective vertebrae V1, V2, V3. Movable joints are advantageously formed at the points where the attachment extensions 20 and the attachment members 22 are attached/coupled. In at least some embodiments of the present disclosure, the ends of the attachment extensions 20 that are attached/coupled with respect to the respective attachment members 22 include respective pedicle screw heads of conventional structure and function. In some other embodiments of the present disclosure, such ends include types of structure other than that of conventional pedicle screw heads. The movable joints formed between the attachment extensions 20 and the attachment members 22 may advantageously permit relatively unconstrained relative rotation (e.g., global rotation) therebetween, as well as at least some rotation of each attachment member 22 about an axis defined by the corresponding attachment extension 20. The structure and function of the movable joints between the attachment extensions 20 and the attachment members 22 of the respective spine attachment elements 12, 14, 16 will be described in greater detail hereinafter.
The attachment members 22 of the spine attachment elements 12, 14, 16 are generally configured and dimensioned so as to be operatively coupled to known spinal support rods (not shown) such as spinal support rods of conventional structure and having a standard diameter (e.g., from about 5.5 mm to about 6.35 mm, although alternative dimensions may be employed) and that are commonly used in connection with lumbar fusion surgery and/or other spinal stabilization procedures. For example, in accordance with some embodiments of the present disclosure, each of the attachment members 22 is configured to couple to a conventional spinal support rod (not shown) so as to prevent relative movement between the attachment members 22 and the rod in a direction transverse (e.g., perpendicular) to the rod's axial direction of extension, and at least one of the attachment members 22 is further adapted to prevent relative movement between such attachment member 22 and the rod along the rod's axial direction of extension. The particular structures and characteristic functions of the attachment members 22 of the spine attachment elements 12, 14, 16 are discussed in greater detail hereinafter.
Referring now to
With respect to at least one of the attachment members 22, the elongated member 18 is coupled thereto such that motion/translation of the elongated member 18 in the axial direction (i.e., in the direction of the axis 24) relative to such attachment member(s) is substantially limited and/or prevented. This ensures that the elongated member 18 is prevented from freely and/or uncontrollably moving/translating in the axial direction with respect to the spine attachment elements 12, 14, 16 in the context of the overall spinal stabilization system 10. Moreover, in accordance with the embodiment of the present disclosure illustrated in
The elongated member 18 is also similar to conventional spinal stabilization rods in that it is substantially dimensionally stable in the radial direction (e.g., transversely/perpendicularly relative to the axial direction of extension of the elongated member 18 as represented by the axis 24). Accordingly, the elongated member 18 is capable of withstanding radially-directed compression forces imposed by any and/or all of the attachment members 22 either during the process of implanting the elongated member 18 along the spine S (e.g., in response to clamping forces imposed by any attachment member 22 on the elongated member 18) or during in situ use of the spinal stabilization system 10 (the details of such use being described more fully hereinafter). In accordance with at least some embodiments of the present disclosure, the material and structural aspects of the elongated member 18 described herein render the elongated member 18 substantially rigid in axial tension, as well as substantially incompressible when subjected to axially-directed compression forces.
Still referring to
The outer sleeve 36 includes an axial portion 62 and two end caps 64 disposed on opposite ends 66, 68 of the axial portion 62 from each other. The axial portion 62 is substantially circular in cross-section, being characterized by a substantially axially constant inner diameter 70 accommodative of the outer diameter 56 of the second inner sleeve 34, a radial thickness 72, and the outer diameter 28, which is further substantially axially constant. At least when the axial portion 62 is in a straight and/or linear configuration, both an inner surface 74 and a peripheral outer surface 76 of the axial portion 62 are substantially cylindrical. The end caps 64 are substantially hemispherical in shape, being characterized by a substantially constant inner radius 78, a radial thickness 80, and a substantially constant outer radius 82 that is of an extent complementary to that of the outer diameter 74 of the axial portion 62.
In at least some embodiments of the present disclosure, including the embodiment schematically depicted herein, the rod 30, the first and second inner sleeves 32, 34, and the outer sleeve 36 are each fabricated from a superelastic material, e.g., such as a nickel titanium alloy. The significance of such material compositions of these components is described more fully hereinbelow.
The rod 30 extends substantially the entire length of the elongated member 18 along the axis 24, beyond the ends 66, 68 of the axial portion 62 of the outer sleeve 36, and into the interior spaces defined by the end caps 64 thereof, e.g., substantially as far as the inner wall surfaces thereof. The rod 30 is also of unitary construction throughout its length and cross-section. Combined with the inherently compact circular shape of the rod 30 in cross section, the superelastic material composition and unitary construction of the rod 30 render it substantially radially incompressible. The first and second inner sleeves 32, 34 extend substantially the full axial distance between the inner wall surfaces of the end caps 64, being only slightly shorter than the rod 30 so as to accommodate the respective radiused geometries of the end caps 64. The cumulative transverse extent of the diameter 38 of the rod 30, the radial thickness 44 of the first inner sleeve 32, and the radial thickness 54 of the second inner sleeve 34, represents a substantial proportion of the transverse extent of the inner diameter 60 of the axial portion 62 of the outer sleeve 36. More particularly, the radial/peripheral spaces between the rod 30 and the first inner sleeve 32, and/or between the first and second inner sleeves 32, 34, are relatively small. At the same time, the above-described coordination among the various diameters of the axially-extending structures of the elongated member 18 is also designed so as to reduce and/or eliminate any undue interference (e.g., via friction or otherwise) with the flexure-related functions of the elongated member 18, which functions are described more fully hereinbelow.
At least in part because of the closely matched diametrical dimensions of the rod 30 and the first inner sleeve 32, the rod 30 substantially fully supports the first inner sleeve 32 against crushing, buckling, and/or plastic deformation during bending, flexure, and/or deflection of the overall elongated member 18 (e.g., during in situ use and/or during representative mechanical testing). For example, in accordance with at least some embodiments of the present disclosure, the attachment members 22 associated with the spine attachment elements 12, 14, 16 apply radial compression, radial impingement, and/or clamping forces to the elongated member 18 at their respective points of contact therewith, and the rod 30 provides structural and/or shape support to the first inner sleeve 32 at, along, and/or adjacent to such points of contact. The first inner sleeve 32, being substantially fully supported against undue radial deflection or deformation (see above), provides similar structural and/or shape support to the second inner sleeve 34. So, in turn, does the second inner sleeve 34 provide structural and/or shape support to the axial portion 62 of the outer sleeve 36. Accordingly, the overall elongated member 18 is substantially radially incompressible along its entire axial length (e.g., along the axis 24), e.g., as against such bending stresses, radial impingement, and/or clamping or other transverse/radial forces as are applied to the elongated member 18, whether by the attachment members 22, or otherwise.
In operation, e.g., when incorporated in the spinal stabilization system 10 adjacent the spine S of a patient as described hereinabove, the elongated member 18 is capable of supporting the spine S in any one or more, or all, of spinal flexion, spinal extension, and axial rotation. As may be seen by comparing
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Further with reference to each of
Referring still further to
It should be appreciated that numerous advantages are provided by the elongated member 18 and/or by devices such as the spinal stabilization device 10 that incorporate the elongated member 18 in accordance with the foregoing description to provide dynamic stabilization to the spine of a patient. Spine surgery patients whose conditions indicate that they would benefit from retaining at least some spinal motion in flexion, extension and/or axial rotation may benefit through implantation of the dynamic spinal stabilization device 10 rather than undergoing procedures involving substantial immobilization as between adjacent vertebrae. The elongated member 18 (e.g., by virtue of its standard diameter sizing, substantial dimensional stability, and rigidity in tension and/or compression) is compatible with most rod attachment hardware presently being implanted in conjunction with lumbar fusion surgery and other spinal procedures, providing at least some basic similarity between the spinal stabilization device 10 and existing spinal stabilization devices. Such similarity is advantageous insofar as it tends to simplify the process of seeking widespread industry acceptance and/or regulatory approval. Exemplary embodiments of elongated member 18 are adaptable to pedicle screw attachment or other mounting systems (e.g., hooks, plates, stems and the like), allow for use across two or more spinal levels, permit at least approximately three to seven degrees of lateral flexibility in spinal extension, spinal flexion, and/or spinal lateral bending as between adjacent spinal vertebrae, and allow for adjustable pedicle screw attachment points along the elongated member 18 to accommodate differing patient anatomies.
The axially symmetrical structure of the elongated member 18 affords an even, predictable level of bending flexibility (or, conversely, bending stiffness) in all lateral directions to facilitate smooth bending, and defines a substantial outer diameter compatible with the same conventional spine attachment hardware normally used in conjunction with solid, substantially laterally inflexible support rods. At the same time, the elongated member 18 is substantially radially incompressible, such that it maintains an adequate degree of rigidity against axial forces in compression (as well as in tension) for purposes of spinal support/stabilization. The peripheral outer surface 76 of the elongated member 18 has a regular cylindrical shape, facilitating secure coupling with hardware designed for coupling to cylindrically-shaped support rods of full diameter and substantially unitary structure. The superelastic material from which the different axially-extending components of the elongated member 18 may be fabricated (at least in part) resists buckling, distension, elastic deformation, and/or galling, and has excellent memory such that the bends produced in the elongated member 18 will be substantially fully removed in the event outside forces acting upon the elongated member are eliminated. Full encapsulation of all other axially-extending components of the elongated member 18 within the axial portion 62 and the end caps 64 of the outer sleeve 36 reduces and/or eliminates the risk that particulate matter, e.g., from metal-metal interaction, will be released in situ. The outer sleeve 36, being fabricated from a superelastic material, includes an inherent degree of stiffness against bending, at least to the extent that its cylindrical shape is supported and/or preserved during bending, flexure, and/or deflection of the elongated member 18. Accordingly, the radial thickness 72 of the axial portion 62 of the outer sleeve 36 can be pre-selected based on that proportion of the bending stiffness of the elongated member 18 which is intended to be supplied by the outer sleeve 36 itself.
It should also be noted that the elongated member 18, and/or the dynamic spinal stabilization device 10 of which the elongated member 18 forms a part, are subject to numerous modifications and/or variations. For example, the elongated member 18 can be attached in many different ways to the attachment members 22 of the respective spine attachment elements 12, 14, 16, including embodiments wherein at least one of the attachment members 22 includes an axial hole through which the elongated member 18 either extends freely in the axial direction, or is clamped in place so as to prevent relative axial motion/translation, and embodiments wherein at least one of the attachment members 22 forms a hook-like structure that includes no clamping means and therefore does not limit axial relative motion/translation of the elongated member 18. Many other variations in the spine attachment elements 12, 14, 16 are also possible, including the number of same provided in the context of the spinal stabilization device 10 (e.g., only two, four or more, etc.), as well as the method by which any or all are attached to their respective spinal vertebrae. The elongated member 18 can accordingly be shortened or lengthened, so as to be suitable for spanning a single pair of adjacent vertebrae, or more than three adjacent vertebrae. The number of inner sleeves can be only one, or more than two, and the diameters thereof, and/or of the rod 30, can be changed as necessary, and/or as desired, e.g., so as to produce a particular (e.g., predefined) amount of bending stiffness in the elongated member 18.
The spinal stabilization system 10 of
Elements illustrated in
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In
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In operation, the rod 3136 can connect to spine attachment elements along axial locations 3158, 3160 disposed at opposite ends of an axial portion 3162 of the rod 3136 in which the channels 3150 are formed. Bending, flexure, and/or deflection of the rod 3136 is permitted substantially only at/along the numerous axially-disposed extents 3152 without risk of plastic deformation of the material of the rod 3136. By cutting/forming channels 3150 of an appropriate number and to an appropriate depth in the rod 3136, the overall bending stiffness of the rod 3136 can be reduced to a predetermined level. Because of the regular radial arrangement of the first, second, third, and fourth series 3142, 3144, 3146, 3148 of channels 3150, the flexibility produced thereby in the rod 3136 is substantially even as to any and/or all transverse directions of bending, flexure, and/or deflection.
Referring now to
The channels 3180 are relatively wider than the channels 3150 (
In operation, the rod 3166 can connect to spine attachment elements along axial locations 3190, 3192 disposed at opposite ends of an axial portion 3194 of the rod 3166 in which the channels 3180 are formed. Bending, flexure, and/or deflection of the rod 3166 is permitted substantially only at/along the numerous axially-disposed extents 3182 without risk of plastic deformation of the material of the rod 3166. The relatively wider dimensions of the extents 3182 produce relatively less flexibility in the rod 3166 than the relatively narrower dimensions 3152 produce in the rod 3136 (
It will be understood that the embodiments of the present disclosure are merely exemplary and that a person skilled in the art may make many variations and modifications without departing from the spirit and scope of the invention. All such variations and modifications, including those discussed above, are therefore intended to be included within the scope of the present invention as described by the following claims appended hereto.