1. Field of the Invention.
The present invention relates generally to medical methods and apparatus. More particularly, the present invention relates to methods and devices for restricting spinal flexion in patients having back pain or other spinal conditions.
A major source of chronic low back pain is discogenic pain, also known as internal disc disruption. Patients suffering from discogenic pain tend to be young, otherwise healthy individuals who present with pain localized to the back. Discogenic pain usually occurs at the discs located at the L4-L5 or L5-S1 junctions of the spine (
This pain experienced by patients with discogenic low back pain can be thought of as flexion instability, and is related to flexion instability that is manifested in other conditions. The most prevalent of these is spondylolisthesis, a spinal condition in which abnormal segmental translation is exacerbated by segmental flexion. The device described here should as such also be useful for these other spinal disorders associated with segmental flexion, for which the prevention or control of spinal segmental flexion is desired.
Current treatment alternatives for patients diagnosed with chronic discogenic pain are quite limited. Many patients follow a conservative treatment path, such as physical therapy, massage, anti-inflammatory and analgesic medications, muscle relaxants, and epidural steroid injections, but typically continue to suffer with a significant degree of pain. Other patients elect to undergo spinal fusion surgery, which commonly requires discectomy (removal of the disk) together with fusion of adjacent vertebra. Fusion is not usually recommended for discogenic pain because it is irreversible, costly, associated with high morbidity, and of questionable effectiveness. Despite its drawbacks, however, spinal fusion for discogenic pain remains common due to the lack of viable alternatives.
Recently, a less invasive and potentially more effective treatment for discogenic pain has been proposed. A spinal implant has been designed which inhibits spinal flexion while allowing substantially unrestricted spinal extension. The implant is placed over one or more adjacent pairs of spinal processes and provides an elastic restraint to the spreading apart of the spinal processes which occurs during flexion. Such devices and methods for their use are described in U.S. Patent Application 2005/02161017A1, published on Sep. 29, 2005, and having common inventors with the present application.
As illustrated in
Ideally, the compliance members 16 will remain horizontally aligned and spaced generally between the spinous processes SP4 and SP5. In some instances, however, the desired symmetry may be lost if the implant structure 10 becomes circumferentially displaced about the spinous processes SP4 and SP5. Such displacement can affect the ability of the implant to provide a uniform, symmetric elastic force to inhibit flexion of the spinous processes of a spinal segment in accordance with the desired treatment. Also, the symmetric designs illustrated in
For these reasons, it would be desirable to provide improved spinal implants and methods for their use in inhibiting flexion in patients suffering from discogenic pain. It would be particularly desirable if the improved devices would provide the desired elastic forces to the spinous processes with minimal risk of displacement or loss of symmetry of the device over time. It would be further desirable if the designs facilitated percutaneous delivery from the side and other approaches.
Additionally, it would be advantageous if the implants and implantation methods could be performed with minimum tissue disruption via percutaneous and open surgical procedures. At least some of these objectives will be met by the invention as described hereinbelow.
2. Description of the Background Art
US 2005/0216017A1 has been described above. US 2006/0271055 describes a spacer having superior and inferior anchors and a spacer element therebetween. Other patents and published applications of interest include: U.S. Pat. Nos. 4,966,600; 5,011,494; 5,092,866; 5,116,340; 5,282,863; 5,395,374; 5,415,658; 5,415,661; 5,449,361; 5,456,722; 5,462,542; 5,496,318; 5,540,698; 5,609,634; 5,645,599; 5,725,582; 5,902,305; Re. 36,221; 5,928,232; 5,935,133; 5,964,769; 5,989,256; 6,053,921; 6,312,431; 6,364,883; 6,378,289; 6,391,030; 6,468,309; 6,436,099; 6,451,019; 6,582,433; 6,605,091; 6,626,944; 6,629,975; 6,652,527; 6,652,585; 6,656,185; 6,669,729; 6,682,533; 6,689,140; 6,712,819; 6,689,168; 6,695,852; 6,716,245; 6,761,720; 6,835,205; Published U.S. Patent Application Nos. US 2002/0151978; US 2004/0024458; US 2004/0106995; US 2004/0116927; US 2004/0117017; US 2004/0127989; US 2004/0172132; US 2005/0033435; US 2005/0049708; US 2006/0069447; Published PCT Application Nos. WO 01/28442 A1; WO 02/03882 A2; WO 02/051326 Al; WO 02/071960 A1; WO 03/045262 A1; WO 2004/052246 A1; WO 2004/073532 A1; and Published Foreign Application Nos. EP 0322334 A1; and FR 2 681 525 A1.
The present invention provides spinal implants and methods for restricting flexion of spinal segments for the treatment of discogenic pain and other spinal conditions, such as spondylolisthesis, where a physician may desire to control segmental flexion. Systems according to the present invention include spinous process constraint structures comprising a first attachment element adapted to be placed over a first spinous process, a second attachment element adapted to be placed over a second spinous process, and a single connector joining the first attachment element and the second attachment element. By “single connector,” it is meant that the connector joins a single point or location on the first attachment element to a single point or location on the second attachment element. In contrast, the prior connectors shown in
The single connector may comprise a single elastic member, where the single elastic member may itself comprise a continuous length of elastic material having uniform or non-uniform elastic properties along said length. Alternatively, the connector may comprise an elastic member including two or more separate components, for example inelastic or non-compliant straps, cables, or other flexible members attached to a compliance member which provides the desired elasticity. Different embodiments for the compliance members are described in co-pending, commonly owned application Ser. No. 12/106,103 (Attorney Docket No. 026398-000410US), filed on Apr. 18, 2008, the full disclosure of which is incorporated herein by reference. Regardless of the particular structure, the single connector and/or elastic member will provide an elastic stiffness in tension between the attachment members in the range from 7.5 N/mm to 50 N/mm, preferably from 10 N/mm to 25 N/mm, and usually in the range from 10 N/mm to 15 N/mm. In addition to providing such elastic stiffness in tension, the single connector and/or elastic member will be constructed to provide little or no elastic stiffness in compression. Usually, the elastic stiffness in compression will be below 3 N/mm, preferably below 0.5 N/mm. The ability of the constraint structures of the present invention to provide a targeted elastic stiffness in tension while providing little or no elastic stiffness in compression allows for treatment of patient's having spinal segments where the kinematics are improved by application of the elastic force to the spine in flexion while providing little or no elastic resistance to extension.
The first and second attachment elements may have similar or different geometries. Exemplary geometries include open hook structures which may be placed about the spinous processes and which have a single attachment point for connection to the single connector. The attachment elements may also be loop structures which fully circumscribe the spinous process, where the loop is provided with a single connection point for connection to the single connector. Often, the attachment elements will be placed over the spinous process without further attachment. In other instances, however, it may be desirable to provide a secondary attachment to the spinous process, such as staples, pins, screws, sutures, adhesives, energy-mediated attachments (such as laser welding), or the like. In some instances, one of the two attachment elements may be adhered to the adjacent spinous process while the other of the attachment elements may be simply placed over the adjacent spinous process without adherence.
The constraint structures of the present invention may comprise separate components which are joined or connectable together. For example, each of the first attachment element, the second attachment element, and the single connector may be formed separately and interconnected by conventional techniques, such as screwing, welding, linking with male and female attachment members, strapping, soldering, or any other such fastening technique. In other instances, any two or more of the components of the constraints of the present invention may be integrally or monolithically formed from a common structural member. For example, a pair of hook-like elements may be integrally formed with an intermediate connector by forming the components from a single rod, wire, cable, polymer substrate, or the like.
The constraint structures of the present invention may be symmetric or asymmetric. For example, when loops or other attachment elements circumscribe the spinous processes the connector may comprise a single axial member lying on the midline or mid-plane which bisects the spinous processes. Such a symmetric structure is advantageous since it applies an axial force generally free from lateral components to the loops which constrain the spinous processes.
In other instances, however, it will be desirable to position the single connector on a side of the spinous processes so that the connector does not need to pass through the region between the spinous processes. Such asymmetric constraint structures thus reduce or eliminate the need to penetrate the interspinous/supraspinous ligaments lessening patient trauma and facilitating placement protocols. For such asymmetric designs, the attachment member may be a simple pin, screw, or other fastener which penetrates the body of the spinous process, but will more usually be a hook, loop, or other member which can attach to the spinous process without necessarily penetrating therethrough. For example, when using hooks, the upper attachment member can be placed over a superior surface of the superior spinous process while a lower hook member may be placed around the inferior surface of the inferior spinous process.
When a single connector lies asymmetrically relative to the plane of the spinous processes, the connector will place the attachment members under a rotational load, often causing the single connector to bow inward toward the spinous process plane. Such deformation of the single connector will also tend to rotate and displace the attachment members, particularly those which are not fixedly attached to the spinous processes. In order to reduce such deformation and improve the stability of the spinous process constraints, a reinforcement member may be placed on or over the single connector, particularly within the region between the spinous processes. For example, a reinforcement sleeve may be placed coaxially over at least a portion of the single connector. Alternatively, and particularly when a compliance member is included in the single connector (as described in more detail below) the reinforcement member may be a slide assembly which is attached to the connector at a superior location and an inferior location and which can extend and contract together with elongation and contraction of the single connector while still maintaining alignment between the superior and inferior segments thereof.
In another aspect of the present invention, the attachment members may be hinged or pivotally connected to the single connector to facilitate introduction and implantation of the constraint structure in a patient. For example, superior and inferior hooks may be pivotally attached at the upper and lower ends of a single connector so that the hooks may be folded to reduce the profile of the constraint as it is being introduced into position adjacent to the spinous processes. Once in position, the hooks or other attachment members may then be pivoted or otherwise moved into place around the spinous processes to provide the desired constraint.
In yet another specific aspect of the present invention, the attachment members may comprise clamps or similar structures which may be placed over posterior surfaces of the spinous processes to hold a single connector therebetween. Such posterior access is advantageous since it reduces the need to disrupt the/supraspinous ligament. Thus the use of clamps or attachment members which are placed over the posterior surface of the spinous processes is particularly advantageous when used in connection with an asymmetric single connector so that the penetration of the supraspinous/ligaments is minimized.
The spinous process constraints of the present invention may further comprise a compliance member disposed within or as part of the single connector. The compliance member may have any structure which provides for the desired elasticity in the connector to permit the first and second attachment elements to spread apart as the spinal segment undergoes flexion. Suitable compliance members are described in published U.S. Application No. 2005/0216017 A1, which has been previously incorporated herein by reference.
In other embodiments, the single connector may comprise an elastomeric body which is disposed between the first and second attachment elements. In some instances, the elastomeric body may be positionable over the supraspinous ligament, and in certain of those cases such elastomeric bodies may be adapted to be sutured or otherwise attached to the supraspinous ligament.
In a further aspect of the present invention, methods for restricting flexion of a spinal segment comprise positioning a first attachment element on a first spinous process and positioning a second attachment element on a second spinous process, wherein the attachment members are joined by a single connector. The attachment members may be positioned in an open surgical procedure through the supraspinous ligament or may be percutaneously implanted, optionally from a single sided posterior approach avoiding the need to penetrate the supraspinous ligament. In a specific embodiment, the elements are joined with an elastic member, where the elastic member is preferably positioned over the supraspinous ligament. In particular embodiments, the methods further comprise attaching the elastic member to the supraspinous ligament, for example by suturing. Usually, the methods further comprise penetrating the supraspinous ligament to permit passage of the attachment element(s) and/or the elastic member therethrough. Still further optionally, the attachment members may be attached to the spinous processes, typically by stapling or any of the other attachment modalities described above.
The novel features of the invention are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings of which:
Referring now to
The first and second attachment members 22 and 24 may be wrapped around the associated spinous process SP4 and SP5 without further adherence or fastening. In some cases, however, it may be desirable to staple, suture, glue, or otherwise attach the attachment members to the underlying spinous process. It will also be appreciated that in many instances the attachment members may have a seam or closure which allows them to be wrapped around the spinous process and closed in situ thereover during an implantation procedure. It will be further appreciated that the single connector 26 may be preattached to either or both of the attachment members 22 and 24. In other instances, however, it may be desirable to attach the connector 26 to either or both of the attachment members 22 and 24 during the implantation procedure in order to permit the length of the connector to be adjusted. In particular, it will be desirable that the length of the connector 26 be selected so that the connector is generally fully extended but not under significant tension when the spinal segment is in its neutral (non-flexion and non-extension) condition. In such cases, the connector 26 will begin to apply tension on the spinous processes 22 and 24 as soon as they begin to undergo flexion while collapsing and applying no force on the spinous processes as they undergo extension.
Referring now to
Referring now to
Referring now to
The spinous process constraint 60 of
Similarly, as shown in
The spinous process constraint 70 of
In still another embodiment, a spinous process constraint system 80, as shown in
side. It will be appreciated that the connector 86 could just as well have been attached laterally on the opposite side.
Referring now to
As described thus far, spinous process constraint systems have been intended to be placed on adjacent spinous processes. It will be appreciated that the constraint systems could be placed on spinous processes which are non-adjacent; e.g., separated by one or more additional spinous processes. It will be further appreciated that the spinous process constraint systems could be attached at a first or upper end to the spinous process SP5 of L5 and at a second or lower end to the sacrum S, as shown in
Referring now to
Referring to
Referring to
Other asymmetric spinous process constraint structures may be constructed in accordance with the principles of the present invention. As shown in
As shown in
While the above is a complete description of the preferred embodiments of the invention, various alternatives, modifications, and equivalents may be used. Therefore, the above description should not be taken as limiting the scope of the invention which is defined by the appended claims.
While preferred embodiments of the present invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the following claims define the scope of the invention and that methods and structures within the scope of these claims and their equivalents be covered thereby.
This application is a divisional of U.S. patent application Ser. No. 12/426,167 (Attorney Docket No. 41564-703.502), filed on Apr. 17, 2009, which is a continuation-in-part of PCT Application US2007/081815 (Attorney Docket No. 026398-000130PC), filed on Oct. 18, 2007, which claimed the benefit of Provisional Application No. 60/862,085 (Attorney Docket No. 026398-000100US), filed on Oct. 19, 2006, the full disclosures of which are incorporated herein by reference.
Number | Date | Country | |
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60862085 | Oct 2006 | US |
Number | Date | Country | |
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Parent | 12426167 | Apr 2009 | US |
Child | 13455917 | US |
Number | Date | Country | |
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Parent | PCT/US2007/081815 | Oct 2007 | US |
Child | 12426167 | US |