Embodiments of the present invention relate generally to a protective sheath covering a portion of a tensioning element such as a wire that makes direct contact with bone, preventing the tensioning element from abrading and damaging the bone surface when the tensioning element is under tension.
Sternotomy is a surgical procedure to access intrathoracic structures such as the heart, whereby the sternum and the attached rib appendages are separated in half along the longitudinal axis of the sternal bone with a saw. The result of sternotomy is illustrated in
To repair the human chest wall following sternotomy, some pass a series of surgical wires in a looped fashion around the sternal halves. This is illustrated in
Additional wires 102 are placed around the sternum 111 repeating the same procedure, with the wires 102 spaced to pass though similar gaps or intercostal spaces 117 between attached ribs 113. By this method, the wires 102 are generally parallel to one another, however, other wiring techniques are commonly practiced such as crossing wires analogous to a shoelace pattern. Furthermore, it is also not unusual for surgeons to place two wires side by side when concerned about poor bone quality or other patient factors such as obesity that might predispose wire to damage and abrade bone. In such instances, it is thought that adding additional wires can assist in counteracting higher biomechanical stresses, cooperating to prevent abrasion and damage to the delicate underlying sternal bone.
Due to the inherent soft nature of sternal bone, the high tension required to restrict the movement of the sternal segments and other patient factors such as high BMI, age, compromised bone health and numerous other underlying comorbidities, wire can easily abrade and damage the sternal bone surface delaying or interfering natural healing. Such abrasion and damage can lead to wire loosening, wire breakage, non-union (unhealed bone), and infection. Such complications might necessitate rehospitalization and surgical intervention to mitigate.
In most cases, wire fixation has proven to be a successful and cost effective method of repairing the cut sternum with minimal reports of infection and non-union. Complication rates (such as for infection and/or non-union) are as high as 8%. Patients that incur complications, however, endure significant pain and resolving their issues has proven difficult, time consuming, and expensive. Surgical wire is thin with minimal surface area which contributes to its propensity to abrade and damage the bone surface, and exposed wire can create a “cheese cutter effect.” Furthermore, many other commonly marketed products tend to be over engineered, complicated, and time-consuming to implant.
A sheath, a sheath assembly, and methods of using the same are provided. A tensioning element such as a surgical wire may be received in a sheath to form a sheath assembly. The sheath may cover some or all of the tensioning element to reduce or prevent the possibility of direct contact between the tensioning element and a bone. By doing so, the sheath may reduce or prevent the tensioning element from abrading and damaging the bone surface when the tensioning element is under tension. The sheath may also reduce the possibility of abrasion and damage to bone when nominal and peak physiologic loads are exerted on the bone. The sheath substantially increases the surface area of contact on the bone and therefore dissipates stresses in an improved manner compared to a tensioned exposed tensioning element.
Furthermore, by providing the sheath, a sheath assembly may be easily customized to fit appropriately on a given bone. The sheath may be bent in some instances to easily conform to the bone surface, allowing the tensioning element to be tightened around a bone while reducing the likelihood of direct contact between the tensioning element and the bone. Relief areas may be provided in some instances to increase the ease of bending the sheath. Furthermore, the sheath may have one or more teeth in some instances to assist in improving traction with the bone. The sheath may be quickly and easily added to a tensioning element and secured around a bone.
In an example embodiment, a sheath is provided. The sheath has a core channel that is configured to receive a tensioning element. The tensioning element is configured to circumscribe a bone, and the sheath is configured to be placed around a bone when the tensioning element received in the core channel circumscribes the bone. The sheath is configured to prevent direct contact between the tensioning element and the bone as the tensioning element is tensioned.
In some embodiments, the sheath may be configured to completely envelop the core channel. However, in some embodiments, the sheath may be configured to only partially envelop a portion of the core channel so that the core channel is partially exposed. In related embodiments, the sheath may have a non-uniform cross section. Further, the sheath may have a buckle, and the buckle may be configured to assist in guiding placement of the tensioning element in the core channel. The buckle may be configured to prevent inadvertent disengagement of the tensioning element from the sheath.
In some embodiments, the sheath may have a non-uniform cross section. In related embodiments, the sheath may have at least one relief area having less material as compared to a remaining portion of the sheath. Further, the relief area(s) may be configured to increase the ease of bending the sheath. Additionally, in some related embodiments, the sheath may contain at least one of a honeycomb pattern, a square grid pattern, round weepholes, or an asymmetrical pattern. Furthermore, in some embodiments, the relief area(s) may be configured to increase the ease of trimming the sheath to a desired length.
In some embodiments, the sheath may have a non-uniform cross section. Further, the sheath may have at least one relief area having less material as compared to a remaining portion of the sheath. The relief area(s) may be configured to permit free passage of blood and other biologic fluids to pass through to reach the fracture site and contribute to biological healing.
In some embodiments, the sheath may include malleable material, and the sheath may be configured to conform to the contour of the bone when the sheath circumscribes the bone. Additionally, in some embodiments, the sheath may have a tapered end, and the tapered end may be configured to reduce resistance as the sheath is pulled through the body.
In another example embodiment, a sheath assembly is provided. The sheath assembly includes a tensioning element and a sheath having a core channel. The core channel is configured to receive the tensioning element. The sheath is configured to be placed around and positioned against a bone, and the sheath is configured to reduce direct contact between the tensioning element and the bone.
In some embodiments, the tensioning element may include at least one bead. The bead(s) may have an increased thickness compared to a remainder of the tensioning element. The bead(s) may be configured to restrain movement of the tensioning element relative to the sheath.
In some embodiments, the tensioning element may be a metal wire, and the tensioning element may have two free ends. The tensioning element may be configured to be tensioned by twisting the two free ends of the tensioning element together, and tensioning of the tensioning element may compress the sheath against the bone. In some related embodiments, the sheath may include malleable material, and the sheath may be configured to conform to the contour of the bone when the sheath circumscribes the bone.
In some embodiments, the sheath may have a non-uniform cross section. In some related embodiments, the sheath may have at least one relief area having less material as compared to a remaining portion of the sheath, and the relief area(s) may be configured to increase the ease of bending the sheath.
In some embodiments, the sheath may have a non-uniform cross section, and the sheath may have at least one relief area having less material as compared to a remaining portion of the sheath. The relief area(s) may be configured to permit free passage of blood and other biologic fluids to pass through to reach the fracture site and contribute to biological healing.
In another example embodiment, a method is provided for applying a sheath assembly. The method includes providing a tensioning element; providing a sheath having a core channel; receiving the tensioning element in the core channel of the sheath; positioning the tensioning element and the sheath around a bone; and securing the tensioning element and the sheath relative to the bone. In some embodiments, securing the tensioning element and the sheath relative to the bone may include applying one or more spikes to the bone.
Having thus described the invention in general terms, reference will now be made to the accompanying drawings, which are not necessarily drawn to scale, and wherein:
Example embodiments of the present invention now will be described more fully hereinafter with reference to the accompanying drawings, in which some, but not all embodiments of the invention are shown. Indeed, the invention may be embodied in many different forms and should not be construed as limited to the example embodiments set forth herein; rather, these embodiments are provided so that this disclosure will satisfy applicable legal requirements. Like reference numerals generally refer to like elements throughout (with the exception of elements shown in
An example of one sheath assembly is illustrated in
As illustrated in
The tensioning element 202 may be a metal wire in some embodiments. Metal wire is relatively inexpensive, efficient and efficacious in most instances when used to close the chest wall following sternotomy. Where the tensioning element 202 is a metal wire, tensioning of a wire covered by a sheath through joining and twisting of its opposing ends may cause the wire and sheath 204 to deform to meet the bone surface. The tension also compresses the wire against the sheath 204, preventing the wire from separating or moving away from the sheath 204 so their relative position and contact to one another is maintained. Where a sheath 204 is used in conjunction with such a wire, this combination may maintain the benefits of using a metal wire while reducing the risk of abrasion from the wire and other risks.
The tensioning element 202 may come in other forms as well. In some embodiments, the tensioning element 202 may be a cable such as a multi-filament cable. Such multi-filament cables may be used in orthopedic applications and may also be used for repairing a severed sternum. Where such a cable is used as the tensioning element 202, the cable may be tensioned and united using tensioning instruments, crimping instruments, and/or crimping sleeves. However, the tensioning element 202 may take other forms. For example, the tensioning element 202 may be a monofilament cable, a cable tie, a strap fastener, another fastener, etc., and the sheath 204 may be configured to fully or partially envelop the tensioning element 202. The tensioning element 202 may comprise a wide variety of materials, including but not limited to stainless steel, titanium, nitonol, resorbable polymeric material, and/or non-resorbable polymeric material. In some embodiments, the tensioning element 202 may include polyether ether ketone (PEEK), polyurethane, nylon, polyethylene, silicone, plastic material, ceramic materials, or other materials. The tensioning element 202 may be formed through thermoforming, 3D printing, or other approaches.
The sheath 204 may have a variety of shapes having different lengths, widths, and cross-sectional shapes. For example, the sheath 204 may have a shape that mimics the shape/form of the underlying tensioning element 202. For example, the sheath 204 may include of a body that is round/cylindrical in shape. However, the sheath 204 may have other shapes. For example, the sheath 204 may be quadrangular (square or rectangular) with or without radiused contours to minimize soft and hard tissue irritation. Alternatively, the sheath 204 may be oval, parabolic, hexagonal or asymmetrical in shape. In one example, the sheath 204 may the central portion of the tensioning element 202 over a span to be in direct contact with bone providing a wider footprint on the bone contacting aspect of the sheath.
As illustrated in
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As illustrated in
The core channel 210 of the sheath 204 illustrated in
The sheath 204 may be provided with varying predetermined lengths in some embodiments, and a sheath 204 having the desired length may be selected based on the size and shape of a bone and intended application. By providing varying predetermined lengths, an appropriately sized sheath 204 may be selected to minimize the amount of excess sheath material.
The sheath 204 and the tensioning element 202 may be contoured in a loop around bones having differing shapes. For example, the sheath 204 and the tensioning element 202 may be used to loop around different bones in a person's body or an animal's body, and the shape of a particular bone (e.g. the sternum) may differ from person to person. Thus, the ability to customize the fit of the sheath 204 and the tensioning element 202 may be desirable to optimize the comfort level, to ensure proper recovery, to minimize any pain, and to minimize the risk of infection or further injury.
A sheath assembly 200 may be introduced into the body of a patient and passed around a bone, traveling together simultaneously in a fixed relationship to one another. For example, in sternal fixation, a sheath assembly 200 may be passed around the sternum 111 (see
The sheath 204 may comprise a variety of materials. The sheath 204 may include any FDA approved implant material in some embodiments. For example, the sheath 204 may comprise polyether ether ketone (PEEK), polyurethane, nylon, polyethylene, silicone, plastic material, ceramic materials, or other materials. In some embodiments, the sheath 204 may include a polymeric based material. The sheath 204 may be flexible and contourable, and this may allow it to conform to the surface of a bone along with a tensioning element 202 passing through a dedicated channel contained within its core channel 210 along its long axis. The sheath 204 may be formed through thermoforming, 3D printing, or using any other method known in the art.
Where a sheath covers a tensioning element 202 from end to end as does the sheath 204, the sheath 204 may be trimmed to expose the tensioning element 202 so that two ends of the tensioning element 202 may be physically joined together. The two ends of the tensioning element 202 may be twisted together by hand or with the assistance of an instrument. Furthermore, the tensioning element 202 may include a needle 201, and the needle 201 may be used to insert the tensioning element 202 through or around cartilage, muscle and other tissues surrounding a bone. The sheath 204 has a uniform cross section that is consistent along the length of the sheath 204, and this cross section is generally circular in shape. However, other cross sectional shapes may be used, and cross sectional shapes may be non-uniform along the length of the sheath 204.
In some embodiments, a sheath assembly may be provided having a sheath that is configured to receive beads of a tensioning element within the core channel of the sheath.
In some embodiments, a sheath may be provided having an exposed channel along its long axis where a tensioning element could rest, as opposed to a tubular configuration in which the entirely of a tensioning element is encased.
Looking first at
Furthermore, providing a bottom surface 313 that is flat may be beneficial to retain the sheath 304 in position, but the bottom surface 313 may have a concave or convex surface in some embodiments. As noted herein, the bottom surface 313 of the sheath 304 may have one or more spiked teeth 728 (see
Turning now to
Looking now a
Where the sheath contains a core channel that is exposed, the channel may have coverage over the tensioning element at periodic points along its long axis. For example, buckles may be provided to assist in guiding the placement of a tensioning element and to help prevent inadvertent disengagement of the tensioning element and the sheath.
In other embodiments, relief areas may be provided in a sheath along the length of the sheath, and the relief areas may aid in the deformation of the sheath to enable the sheath to better conform to the surface of the bone.
Between the sections 620, relief areas 618 may be provided. Intermediate connections 619 may be provided in the relief areas 618 to connect adjacent sections 620 together. To the extent an operator desires to trim a portion of the sheath 604, the operator may trim the sheath at one of the intermediate connections 619. The intermediate connections 619 may generally possess a smaller thickness than the sections 620, making the intermediate connections 619 easier to trim. In some embodiments, the intermediate connections 619 may be manually trimmed at a desired point to trim the sheath 604, and this may be done by applying a sideloading force to the sheath 604 at the location where the breakage is desired. Trimming may be performed either before or after the sheath 604 have been placed inside the body of the patient, and trimming may be performed either before or after any tensioning element 602 has been added to the sheath 604. In the case where the tensioning element 602 has been assembled to the sheath 604 prior to trimming, excess sheath material may be trimmed and separated from the tensioning element 602 by simply sliding the excess sheath material off the tensioning element 602.
The sheath 604 may also include a tapered end 608. The tapered end 608 may aid the placement of the sheath 604 around a bone, reducing drag allowing the sheath 604 to more easily pass though or around cartilage, muscle, and other tissues covering or surrounding a bone.
Furthermore, the sheath 604 may include a bottom surface 613, and the bottom surface may be configured to contact a bone so that a tensioning element 602 placed in the core channel 610 (see
Furthermore,
While the sheath 504 and the sheath 604 illustrate example relief areas 518 and 618, relief areas may be provided in other ways. For example, relief areas may be provided in a honeycomb pattern, a square grid pattern, with round weepholes, or in an asymmetrical pattern.
Furthermore, the sheath may include a spike or spiked teeth to assist in restraining movement of the sheath relative to a bone.
The spike 828A may extend the entire length of the sheath 804 as illustrated in
Spikes 828A of
In some embodiments, multiple sheaths 904 may be used within a sheath assembly.
While various sheath assemblies and sheaths have been described herein, methods of using sheath assemblies and sheaths are also contemplated.
At operation 1008, an unwanted portion of the sheath and/or the tensioning element may be trimmed. This may reduce the amount of excess material of the tensioning element and/or sheath material. At operation 1010, the tensioning element and sheath may be positioned around the bone. At operation 1012, the tensioning element and the sheath may be secured relative to the bone. Where the tensioning element is a wire, securing the tensioning element and the sheath relative to the bone may entail twisting the wire to reduce the size of the loop formed by the wire. Additionally or alternatively, securing the tensioning element and the sheath relative to the bone may entail applying the spikes or spiked teeth to the bone to gain traction between the bone and a surface of the sheath.
It should be understood that the operations discussed for the method 1000 may be performed in any order. Furthermore, some operations may be performed simultaneously with one another. Additionally, operations may be added or some operations may be removed. The method 1000 may be performed multiple times so that multiple sheath assemblies may be installed around a bone such as the sternum.
Many modifications and other embodiments of the inventions set forth herein will come to mind to one skilled in the art to which these inventions pertain having the benefit of the teachings presented in the foregoing descriptions and the associated drawings. Therefore, it is to be understood that the embodiments of the invention are not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the invention. Moreover, although the foregoing descriptions and the associated drawings describe example embodiments in the context of certain example combinations of elements and/or functions, it should be appreciated that different combinations of elements and/or functions may be provided by alternative embodiments without departing from the scope of the invention. In this regard, for example, different combinations of elements and/or functions than those explicitly described above are also contemplated within the scope of the invention. Although specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation.
This application claims the benefit of U.S. Provisional Patent Application No. 63/346,577 (filed on May 27, 2022, and entitled “Sheath Assembly for Sternal Wire”), the entire contents of which are hereby incorporated herein by reference for all purposes.
Number | Date | Country | |
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63346577 | May 2022 | US |