The human skeleton is composed of 206 individual bones that perform a variety of important functions, including support, movement, protection, storage of minerals, and formation of blood cells. These bones can be grouped into two categories, the axial skeleton and the appendicular skeleton. The axial skeleton consists of 80 bones that make up the body's center of gravity, and the appendicular skeleton consists of 126 bones that make up the body's appendages. The axial skeleton includes the skull, vertebral column, ribs, and sternum, among others, and the appendicular skeleton includes the long bones of the upper and lower limbs, and the clavicles and other bones that attach these long bones to the axial skeleton, among others.
To ensure that the skeleton retains its ability to perform its important functions, and to reduce pain and disfigurement, fractured bones should be repaired promptly and properly. Typically, fractured bones are treated using fixation devices, which reinforce the fractured bones and keep them aligned during healing. Fixation devices may take a variety of forms, including casts for external fixation and bone plates for internal fixation, among others. Casts are minimally invasive, allowing reduction and fixation of simple fractures from outside the body. In contrast, bone plates are internal devices that mount under the skin of a plate recipient and in engagement with bone to span a fracture.
Trauma to the torso may result in fracture of one or more ribs. Frequently, a simple rib fracture is nondisplaced, so that reduction and/or internal fixation of the fractured rib may not be required. However, in cases of more severe trauma to the chest, a single rib may be fractured more severely and/or multiple rib fractures may occur. With multiple rib fractures, a section of the thoracic wall may become detached from the rest of the chest wall, a condition known to medical practitioners as “flail chest.” Flail chest often results in paradoxical motion of the injured area, in which the freely floating thoracic section is drawn in during inspiration, and pushed out during expiration. This condition may result in severe respiratory distress, possibly requiring the patient to be sedated and/or intubated during early stages of healing. Fixing single or multiple rib fractures internally may alleviate paradoxical motion, reduce pain, and/or help to prevent secondary injuries.
Internal fixation of a rib fracture may be accomplished using a bone plate to span the fracture. A bone plate suitable for treating a fractured rib may be custom-contoured (i.e., bent) by a surgeon to conform to a region of a rib spanning a fracture, and then fastened to the rib on both sides of the fracture. The plate thus fixes the rib to permit healing. The plate may be fastened to the fractured rib using fasteners, such as bone screws. Alternatively, a bone plate may be used that has prongs disposed along its length. The prongs may be crimped so that they grasp the rib to fasten the bone plate to the rib.
Each of these plating techniques may have disadvantages for rib fixation. Installation of a bone plate for fib fixation may require a relatively long incision over a rib, in order to expose a sufficient surface area of the rib for receiving the bone plate. Moreover, many or all of the ribs have segments that are covered by another bone, which makes fixation with a bone plate impractical. For example, a rib fractured near its site of articulation with a vertebra or where it extends under the scapula is difficult to fix with a bone plate. In either case, the fracture site is blocked on its outer side by another bone and thus cannot be easily accessed surgically.
The present disclosure provides systems, including methods, apparatus, and kits, for fixing rib bones with a fixation device including an intramedullary nail connected to a generally U-shaped plate.
The present disclosure provides systems, including methods, apparatus, and kits, for fixing rib bones with a fixation device including an intramedullary nail (also termed an intramedullary rod) connected (or connectable) to a generally U-shaped plate.
To perform a method of fixing a rib bone, a nail member may be placed along a medullary canal of a rib bone to span a discontinuity (a fracture or cut) in the rib bone. A generally U-shaped plate member may be disposed on the rib bone with a pair of arms of the plate member disposed adjacent generally opposing sides of the rib bone, such as respective inner and outer surface regions of the rib bone. The plate member may be attached to the rib bone with at least one fastener, which may extend into and/or through at least one aperture of the plate member and into and/or through the rib bone. In some cases, the fastener may extend to each member of a pair of aligned apertures defined by the pair of arms. The fastener may be a threaded fastener that locks to (achieves a threaded engagement with) the at least one aperture and/or with one or both members of the pair of aligned apertures. The nail member may have a connection to the plate member, at least after, if not before, the nail and plate members are fully installed respectively in and on the rib bone, such that the plate member attached to the rib bone restricts the nail member from migrating in the rib bone, such as to restrict the nail member from backing out of the rib bone. The nail member and the plate member may have a connection to one another before the nail member and the plate member are positioned respectively in and on the rib bone. For example, the nail member and the plate member may be unitary with one another (i.e., provided collectively by one-piece construction), if the members have a connection before installation, or may be provided by discrete nail and plate pieces that are configured to be connected to another before or after the nail and plate pieces are positioned with respect to the rib bone, but typically during installation.
The fixation device may include any suitable structure to facilitate its function and/or installation. For example, the arms of the plate member may be connected by a bridge region, and the nail member may be connected to the plate member centrally along the U-shape defined by the plate member, that is, connected via the bridge region. With this configuration, the nail member may be placed into a rib bone from a superior side of the rib bone. Alternatively, or in addition, the fixation device may include a connector region disposed between the nail member and the plate member, at least after, if not before, the members are fully installed in and on the rib bone. The connector region may be configured to be more flexible than the nail member and/or the plate member such that the fixation device can be deformed selectively in the connector region to change a relative disposition of the nail member and the plate member, which may facilitate placement of the plate member onto the rib bone, with the nail member in the rib bone, and/or may facilitate alignment of nail and plate pieces, among others.
The fixation device and methods of use disclosed herein may solve one or more problems presented by the prior art. These problems may include (1) the tendency of a K-wire or bone screw to migrate or back out of a rib bone (due to the softness and flexibility of the rib bone necessary for breathing), which can result in loss of rib fixation, (2) the inadequate strength of a K-wire for rib fixation, (3) the ability of a migrating K-wire to penetrate and migrate through soft tissue, which may even injure the heart, (4) the inaccessibility of many rib fracture sites for fixation with a bone plate, and/or (5) the relatively long incision and extent of soft tissue injury required for installation of a bone plate on a rib bone.
Further aspects of the present disclosure are described in the following sections: (I) overview of an exemplary fixation system, (II) exemplary methods of fixing a rib bone, (III) nails, (IV) plates, and (V) examples.
Rib bone 42 may include at least one discontinuity (i.e., a fracture 54 or a cut) that is spanned by nail 46 inside the rib bone. The nail may be configured to be disposed longitudinally in the rib bone such that the nail extends along a medullary canal 56 of the rib bone. Any suitable portion or all of the nail may extend along the medullary canal. The nail may enter the rib bone at an entry site 58 on any suitable side or surface region of the rib bone, such as an outer side 60 or a superior side 62, among others.
Arms 70, 72 each may define a member of a pair of aligned apertures, namely, an outer aperture 80 and an inner aperture 82. Threaded fastener 50 may extend through rib bone 42 between apertures 80, 82 and may lock to at least one of the apertures, such as inner aperture 82. Accordingly, inner aperture 82 may include an internal thread. Alternatively, or in addition, inner aperture 82 may be elongate (i.e., a locking slot) as shown here.
Further aspects of plates and locking slots that may be suitable for the fixation devices disclosed herein are described in U.S. Provisional Patent Application Ser. No. 60/934,696, filed Jun. 15, 2007, which is incorporated herein by reference.
The plate and/or the nail of a fixation device may be formed of a biocompatible and/or bioresorbable material(s). Exemplary biocompatible materials that may be suitable include (1) metals (for example, titanium or titanium alloys, alloys with cobalt and chromium (cobalt-chrome), stainless steel, etc.); (2) plastics (for example, ultra-high molecular weight polyethylene (UHMWPE), polymethylmethacrylate (PMMA), polytetrafluoroethylene (PTFE), polyetheretherketone (PEEK), and/or PMMA/polyhydroxyethylmethacrylate (PHEMA)); and/or (3) bioresorbable (bioabsorbable) materials or polymers (for example, polymers of α-hydroxy carboxylic acids (e.g., polylactic acid (such as PLLA, PDLLA, and/or PDLA), polyglycolic acid, lactide/glycolide copolymers, etc.), polydioxanones, etc.). If provided as discrete pieces, the nail and the plate may be formed of the same material or of distinct materials.
This section describes exemplary methods of fixing a rib bone with an intramedullary nail. The method steps described herein and elsewhere in the present disclosure may be performed in any suitable combination and in any suitable order. To aid in understanding the method steps,
A rib bone may be selected for fixation. The rib bone may have a discontinuity (such as at least one fracture and/or a cut, among others) sustained or produced by any suitable injury or procedure. The discontinuity may be disposed medially, laterally, posteriorly, and/or anteriorly on the rib bone. In some examples, the rib bone may have sustained a fracture that is positioned inward of and thus covered by another bone, such as a vertebra or a scapula, among others.
A discontinuity in the rib bone may be reduced. For example, a fractured rib bone may be set. Reduction of the discontinuity may be performed before, during, and/or after a fixation device is attached to the rib bone, but typically before.
An aspect of the rib bone may be measured, generally in the vicinity of the discontinuity. Measurement may be performed with any suitable measuring device or method, such as calipers, a ruler, a tape measure, a fluoroscope (e.g., by fluorography), and/or the like, or any combination thereof, among others. The aspect may correspond to a characteristic dimension of the rib bone, such as thickness, width, length, diameter, or any combination thereof, among others. Alternatively, or in addition, the aspect may correspond to a curvature and/or surface contour of the rib bone, among others.
A fixation device may be selected. The fixation device may include a plate and a nail. The plate and nail may be provided by one piece or may be provided by two or more discrete pieces. The fixation device may be selected from a set of available fixation devices and/or device pieces. For example, the set may include U-shaped plates with different arm-to-arm spacings and/or radii of curvature. In other examples, the set may include nails of different length, diameter, curvature, site of connection to the plate, or any combination thereof, among others. Selection may be performed based on the type, size, and/or contour of the rib bone, among others, and thus may be based on a measured, average, and/or expected aspect (such as thickness) of the rib bone. The nail and/or plate may be manufactured with a predefined size and shape and/or may be custom contoured prior to and/or during installation for a particular rib bone, rib bone region, and/or for the particular anatomy of the patient. Custom contouring (generally, bending) may be performed pre- and/or intraoperatively by hand, with the aid of a tool, and/or with a die, among others.
Nail 46 of fixation device 44 may be placed into the rib bone at least partly along the medullary canal.
The fixation device may be installed as separate pieces or as a one-piece unit. In the case of device 44, nail 46 is already connected to plate 48 as nail 46 is advanced into the rib bone. However, if installed as a unit, the plate of the device may interfere with nail advancement and/or seating of the plate on the rib bone because of premature engagement of the plate with the rib bone. For example, with fixation device 44, if nail 46 is advanced with arms 70, 72 of plate 48 pointing inferiorly, inner arm 72 may be positioned adjacent the outer side 60 of the rib bone and through engagement with the outer side may prevent the nail from being advanced fully. Accordingly, as shown in
The plate may be disposed on the rib bone with a pair of arms of the plate disposed adjacent respective outer and inner surface regions 60, 76 of the rib bone. Disposing the plate may include disposing the bridge region adjacent a superior or inferior surface region of the rib bone. However, placement of the bridge region superiorly may be preferable to avoid the neurovascular bundle disposed inferiorly of a rib bone. In any event, as shown in
The shape of the fixation device and the relative disposition of the nail and the plate may be adjusted at any suitable time by deforming a connector region that connects or will connect the nail and the plate to one another. The connector region thus may facilitate pivoting the plate onto the rib bone, may permit adjustment of the final position of the plate on the rib bone (such as to allow a plate to move inferiorly into contact with the rib bone), and/or may facilitate alignment of a nail piece with a plate piece during installation (e.g., see Example 2).
The plate may have a resiliency that promotes engagement with the rib bone and, optionally, provides attachment of the plate to the rib bone. In particular, the arms of the plate may be biased toward their original spacing by an integral plate spring formed by the plate, which may clamp the plate onto the rib bone. The ends of the arms may be urged or held apart as they are advanced onto the rib bone, and then may be allowed to spring back toward one another to engage the rib bone. In some embodiments, the plate may clamp onto bone via the integral plate spring for attachment without the use of fasteners, although one or more fasteners may be utilized to reinforce attachment. Furthermore, one or more prongs or ridges may be formed on an inner surface of the plate to promote engagement with the rib bone, such as by penetrating the rib bone, to restrict slippage of the clamped plate relative to the rib bone, particularly when the plate is used without fasteners.
If the plate is attached via a fastener(s), on or more transverse holes may be formed in the rib bone for receiving the fastener (e.g.,
The plate may be attached to the rib bone with at least one fastener, such as a threaded fastener(s) and/or a tie mechanism(s), among others. One or more fasteners thus may be selected. The fasteners may be selected, for example, to have a diameter less than the width/diameter of a target aperture of the plate, and, if threaded, to have a thread configuration corresponding to the size/offset of an aperture lip (for an elongate locking aperture) or to the pitch of an aperture thread (for a locking aperture having an internal thread). The fasteners also or alternatively may be selected to have a length (particularly a shaft length for a threaded fastener) that corresponds to a measured or expected thickness of the rib bone. The fastener(s) may be placed through a plate aperture and into a pre-formed hole in the rib bone or may form a hole itself. The fastener may engage the plate adjacent only one side of the rib bone and/or adjacent generally opposing surfaces of the rib bone, among others. Each fastener may extend through the plate or through overlapping plate and nail pieces. In some examples, the fastener may be tightened until the arms of the plate are compressed against the rib bone.
The fixation device may include a nail configured to be placed at least partially along a medullary canal of a rib bone. The nail thus may be elongate with a linear or bent shape. If bent, the nail may have a curvature that is restricted to a plane or that extends to three dimensions. The curvature may be introduced into the nail during manufacture, intraoperatively before placement of the nail into the rib bone, and/or as the nail in placed into the rib bone. Accordingly, the nail may be sufficiently flexible such that the nail adapts to the curvature of the rib bone's medullary canal, via contact with the rib bone, as the nail is advanced along the medullary canal. In any event, the nail may be bent according to the curvature of a rib bone.
The nail may have any suitable length. For example, the nail may have a length that is at least about the same as or greater than the width of the plate defined generally parallel to the long axis of the nail. For example, the nail may be at least about one and one-half, two, three, or four times the width of the plate, among others.
The nail may have any suitable cross-sectional shape and size. For example, the nail may have a cross-sectional shape that is uniform or that varies along the nail. Suitable cross-sectional shapes may include circular, oval, polygonal, or a combination thereof, among others. Accordingly, the nail may be cylindrical or conical along at least a portion, at least most, or at least substantially all of its length. The diameter of the nail may be substantially uniform along the length of the rod or may vary, such as tapering as the rod extends toward its leading end. The nail may have any suitable surface relief structure, i.e., projections and/or recesses formed on the surface of the nail. Exemplary surface relief structure may include longitudinal ridges and/or grooves, dimples, bumps, annular ridges and/or grooves, helical ridges and/or grooves (e.g., an external thread and/or one or more drill flutes (i.e., a self-drilling nail), among others), and/or the like. The nail may have any suitable apertures, such as one or more blind holes and/or through-holes. The apertures may extend longitudinally along and/or completely through the nail, such as to provide a cannulated nail, or may extend transversely into and/or through the nail. Each aperture may be locking (e.g., with an internal thread) or may be nonlocking. The nail may have a transverse dimension (e.g., diameter, width, and/or thickness) corresponding to the diameter of the medullary canal of a rib bone. The nail thus may be about the same size as the medullary canal transversely, may be somewhat oversized in a transverse dimension to provide a tight fit in the rib bone, and/or may be somewhat undersized in a transverse dimension to facilitate sliding the nail along the medullary canal during installation. Accordingly, the nail may have a transverse dimension that is larger than that of a K-wire, namely, greater than about 1.6 millimeters. For example, the nail may have a transverse dimension that is at least about one-fourth or one-half the thickness and/or at least about one-fourth or one-half the width of a rib bone into which the nail is placed. In exemplary embodiments, the nail may be about 3-5 or at least about 2, 3, 4, or 5 millimeters in thickness and about 3-8 or at least about 3, 4, 5, or 6 millimeters in width (or diameter), among others. The nail thus may be bigger, stronger, stiffer, more resilient, more tapered, or any combination thereof relative to a K-wire to provide substantially improved fixation in comparison to a K-wire.
The fixation devices of the present disclosure may include a generally U-shaped plate that connects to a nail. The plate may have a bridge region and arms opposingly flanking and extending away from the bridge region.
The plate may have any suitable spacing, structure, and disposition of its arms. Generally the arms may be spaced about the same as the distance between generally opposing surfaces of a target rib bone, that is, about the width, thickness, and/or diameter of the rib bone where the plate will be disposed. However, in some examples, the arms may be spaced somewhat greater than this distance, at least when the plate is first placed on bone, to facilitate placement. Alternatively, the arms may be spaced somewhat less than this distance, so that the arms of the plate, particularly distal regions of the arms spaced from the bridge region, may be urged farther apart as the plate is placed onto bone. In some cases, the plate may be resilient with a bias to return to its original configuration, such that the arms, if urged apart by bone, tend to opposingly engage the bone due to the bias. The arms may be at least substantially parallel, or may diverge or converge toward their distal ends (spaced from the bridge region). In exemplary embodiments, the arms may have a spacing that corresponds to the thickness of a rib bone.
The plate may have any suitable width. The width of the plate may be generally constant within each arm and/or within the bridge region. Alternatively the width may vary within one or both arms, between the arms, within the bridge region, or between the arms and the bridge region. For example, the arms may taper away from the bridge region. Alternatively, or in addition, the bridge region may be narrower than the arms, to facilitate bending the bridge region (e.g., to facilitate adjustment of the spacing of the arms), or the arms may be narrower than the bridge region (e.g., to facilitate adjustment by bending the arms). In some embodiments, the plate may include one or more narrowed regions, at which the plate may be bent selectively, such as within one or both arms or the bridge region, and/or at a junction between an arm and the bridge region.
The plate may have any suitable thickness. The thickness may be selected based on various considerations, such as reducing the profile of the plate on bone, providing a sufficient strength to restrict movement of the nail, bendability, providing a sufficient thickness to form opposing lips or a thread in an aperture for engaging a fastener thread, and/or the like.
A plate may have any suitable number, shape, and arrangement of apertures. The plate may have no apertures or may define one or more apertures. Each aperture may be circular or elongate, among others. Each aperture may include or lack a counterbore. The apertures may be disposed in the arms and/or the bridge region of the plate. If two or more apertures are included in a plate, the apertures may be arrayed across the width and/or along the length of one or more arms and/or the bridge region, and/or may have a staggered disposition. In some examples, one or more pairs of apertures may be aligned, that is, configured to receive the same fastener with each aperture of the pair. Apertures of an aligned pair may be disposed in the arms and/or in the bridge region and one arm, among others. Each aligned pair of apertures may have zero, only one, or two locking apertures. Apertures of an aligned pair may have the same general shape, such as oval or circular, or may have different shapes, such as oval and circular, among others. Furthermore, apertures of an aligned pair may be of generally the same size, such as about the same length and/or width, or may have different lengths and/or widths. The thickness of the bone plate adjacent the aperture(s) (in the plate and/or other portions of the plate) may be generally the same as, less than, or greater than the thickness of the plate away from the aperture(s). Plate thinning near the apertures may provide a recess for reducing the profile of fasteners placed in the apertures, and plate thickening near the apertures may reinforce the aperture.
Each aperture may be locking or nonlocking. Locking apertures generally include a retention structure to engage a fastener, such as through a thread of the fastener, and restrict axial movement of the fastener in both axial directions. The retention structure may be one or more ridges or lips formed by the wall of a locking aperture. The ridges may be generally helical, to form a thread, at least partially linear to form a locking slot, and/or the like.
The plate may have any suitable surface structure. The surface structure may be formed by an inner surface, an outer surface, and/or a side(s)/edge(s)/end(s) disposed between the inner and outer surfaces. The surface structure may include one or more projections, such as a ridge(s) or bump(s), or one or more depressions, such as a groove(s) or dimple(s). If a projection, the projection may be relatively sharp and/or pointed or may be relatively dull and/or rounded, among others. Exemplary surface structure that may be suitable includes one or more prongs or sharp ridges to engage and/or penetrate bone, one or more projections to space the body of the plate from bone, one or more grooves or notches to receive and retain a suture, and/or the like.
The following examples describe selected aspects and embodiments of the present disclosure. These examples and the various features and aspects thereof are included for illustration and are not intended to define or limit the entire scope of the present disclosure.
This example describes an exemplary fixation system 120 including a fixation device 122 having a nail 46 extending from a central region of U-shaped plate 48; see
Fixation device 122 may be structured for installation from a position superior (or inferior) to a rib bone (e.g., from a position between a pair of adjacent rib bones), such that nail 46 enters the rib bone from a top side or top surface region (or bottom side/surface region) of the rib bone. Device 122 may be utilized to fix any suitable rib injury but in some cases may be utilized advantageously to fix a posterior fracture of a rib bone. For example,
Nail 46 and plate 48 may be structured generally as described above for fixation device 44 (see
This example describes an exemplary fixation system 150 including a fixation device 152 that includes a nail and a generally U-shaped plate formed by discrete pieces; see
Fixation device 152 may be installed generally as described above in Section II. However, since the nail and plate pieces may be positioned separately, the nail piece may be placed into the rib bone at any suitable time relative to disposing the plate piece on the rib bone (i.e., before, during, and/or after).
In other embodiments, a nail piece and a plate piece may be connected to one another by other any suitable fastener mechanism. Exemplary other fastener mechanisms include threaded engagement of the nail and plate pieces with one another or attachment via a threaded fastener locks to one or both of the nail and plate pieces without extending into the rib bone. Further aspects of other suitable fastener mechanisms for connecting plate and nail pieces are described in U.S. Provisional Patent Application Ser. No. 60/934,696, filed Jun. 15, 2007, which is incorporated herein by reference.
This example describes an exemplary fixation system 180 including nail piece 154 connected to a rib bone with a tether 182; see
Nail piece 154 may be placed into the rib bone and held in place with tether 182, instead of or in addition to a threaded fastener and a plate piece. The tether may be a flexible line or strap, such as a suture 184, a wire, or a cable tie (also termed a zip tie), among others. Tether 182 may be placed through through-hole 164 and also through a transverse channel 186 formed in the rib bone. The tether also may extend around at least a portion of the rib bone and may be secured to itself, such as via a knot 188, a retainer, or the like, to form a loop.
This example describes an exemplary fixation device 210 with a flexible connector region created by opposing slits; see
Fixation device 210 may include any of the nail and plate structure described elsewhere in the present disclosure. For example, fixation device 210 may be of one-piece construction with nail 46 connected integrally to U-plate 48 via a flexible connector region 212. The connector region may acquire at least some of its flexibility by transverse slits or openings 214 defined in the fixation device between the nail and the U-plate. The transverse slits may be defined in a plate-like or a rod-like region of the fixation device and thus may extend into the connector region from opposing sides or from three or more positions around the long axis of the nail. In any event, the transverse slits defined from generally opposing sides may be deep enough to overlap one another. In some embodiments, connector region 212 may be resilient such that slits 214 form a serpentine spring, which may flex in a plane or in three dimensions.
The disclosure set forth above may encompass multiple distinct inventions with independent utility. Although each of these inventions has been disclosed in its preferred form(s), the specific embodiments thereof as disclosed and illustrated herein are not to be considered in a limiting sense, because numerous variations are possible. The subject matter of the inventions includes all novel and nonobvious combinations and subcombinations of the various elements, features, functions, and/or properties disclosed herein. The following claims particularly point out certain combinations and subcombinations regarded as novel and nonobvious. Inventions embodied in other combinations and subcombinations of features, functions, elements, and/or properties may be claimed in applications claiming priority from this or a related application. Such claims, whether directed to a different invention or to the same invention, and whether broader, narrower, equal, or different in scope to the original claims, also are regarded as included within the subject matter of the inventions of the present disclosure.
This application is based upon and claims the benefit under 35 U.S.C. § 119(e) of U.S. Provisional Patent Application Ser. No. 60/934,696, filed Jun. 15, 2007, which is incorporated herein by reference in its entirety for all purposes. The following patent documents are incorporated herein by reference: U.S. Provisional Patent Application Ser. No. 60/498,866, filed Aug. 28, 2003; U.S. Provisional Patent Application Ser. No. 60/548,685, filed Feb. 26, 2004; U.S. patent application Ser. No. 10/927,824, filed Aug. 27, 2004, and published as Pub. No. U.S. 2005/0085819 A1 on Apr. 21, 2005; U.S. patent application Ser. No. 11/454,613, filed Jun. 16, 2006, and published as Pub. No. U.S. 2007/0123883 A1 on May 31, 2007; and U.K. Patent Application Serial No. 0810872.2, filed Jun. 13, 2008, titled “Rib Fixation with an Intramedullary Nail,” and naming Joel Gillard and Randall J. Huebner as inventors.
Number | Date | Country | |
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60934696 | Jun 2007 | US |