The present invention is related to the general surgical repair of separated body tissues, and more particularly to internally fixating and stabilizing such body tissues, specifically bones.
In the present state of the art, there are a number of systems available to repair biological tissues separated in surgery or by injury. These products serve to approximate and stabilize the tissues so that healing may commence and provide compression in the interface to promote healing. Compression and stability are critical for proper anatomical healing of tissue. With the correct amount of compression applied to the interface of the tissue portions to be joined, signals are sent to the tissue, thus allowing the tissue to remodel in proper anatomical position. The amount of compression applied to the tissue interface needs to be appropriate to the type of tissue that is being healed.
When it is necessary to access the thoracic cavity for a medical procedure, for example, it is required to cut the sternum into two pieces using a rib spreader. Once the procedure is completed within the thoracic cavity, the sternum must be repaired. For such repairs, it is known to use a dynamic compression device like that shown in
1. Bulky spring materials, while occupying substantial space, often do not store much energy. Some use polymer elastic bands, while other use coiled springs;
2. Wires are sometimes used to wrap the bones into position in compression with one another. However, wires can have sharp ends that can damage adjunctive tissues. Knot stacks in suture can interfere with the natural movement of surrounding tissues; and
3. Current banding systems that incorporate a biasing mechanism to achieve dynamic compression, like the device 14 described hereinbelow, put the biasing mechanism in line with the band or suture. This practice competes with precious space at the healing site. Suture or bands are used to approximate tissues so that they may heal. It is desirable to obtain the best purchase possible on the tissue, so that the binding mechanics offered by the suture may be utilized. The best purchase is optimized by ensuring that the suture has the greatest contact area with the tissue. If a biasing mechanism is interfering with this concept, the biasing mechanism may diminish the suture's ability to hold the tissues together.
What is needed is an improved dynamic compression system which addresses and overcomes these shortcomings in an innovative way.
The present invention solves the problems outlined above by providing a biasing system for a suture or banding system that does not adversely affect the band's ability to hold tissue together. This is done by removing most or all of the biasing mechanism from the path of the band. By placing the biasing mechanism to one or the other side of the tension path of the band, many desirable effects are realized.
The inventor has recognized that maximizing contact between the suture or band and the underlying bone or tissue is important to optimize healing. This is particularly relevant in the case of holding sternal halves together after they have been separated to access the thoracic cavity. Breathing, coughing, and any movement by the upper body impart larger forces in the repair held together by bands. Any biasing device must serve to augment or maintain the function of the bands. If this is not the case, coughing may induce stresses that concentrate on one part of the bone, causing the bands to cut into the bone. When the bands cut into the bone, the tension in the bands is released adversely, thus affecting their ability to help mend bone to bone.
More particularly, there is provided in one aspect of the invention a dynamic tissue holding device for dynamically holding two tissue portions in contact with one another. The device comprises a biasing spring having a relatively low profile, and a band adapted for extending about the tissue portions to be held together. The band has a first end for attachment to a first attachment portion on the biasing spring and a second end for attachment to a second attachment portion on the biasing spring. The band establishes a path of tension along its length and extending linearly between the two ends of the band. Advantageously, more than one-half of the biasing spring is disposed outside of the path of tension when the dynamic tissue holding device is in place and holding the two tissue portions together.
Advantageously, at least approximately four-fifths of the biasing spring is disposed outside of the path of tension. The height of the biasing spring is less than about 2 mm. In one particular embodiment, the biasing spring is formed to have a generally parabolic profile. The band preferably comprises a braided band, or, alternatively, a cable.
In one embodiment of the invention, the biasing spring comprises a first eyelet disposed in a center portion of the spring, for receiving the first end of the tensioning band, and a second eyelet disposed on an opposing side of the center portion of the spring, for receiving the second end of the tensioning band, wherein at least approximately four-fifths of the spring is disposed on either one side or the other of the first and second eyelets. More preferably, approximately two-fifths of the spring is disposed on one side of the first and second eyelets and approximately two-fifths of the spring is disposed on the other side of the first and second eyelets. The space efficiency of the biasing spring is at least about 50%, and preferably at least about 57%.
In another embodiment of the invention, the biasing spring comprises a first eyelet disposed on one edge of the spring, for receiving the first end of the tensioning band, and a second eyelet disposed on a second edge of the spring, for receiving the second end of the tensioning band, wherein substantially all of the biasing spring is disposed to one side of said eyelets.
In another aspect of the invention, there is provided a dynamic tissue holding device for dynamically holding two tissue portions in contact with one another, which comprises a biasing spring and a band adapted for extending about the tissue portions to be held together. The band has a first end for attachment to a first attachment portion on the biasing spring and a second end for attachment to a second attachment portion on the biasing spring. A particularly advantageous feature of the invention is that the aspect ratio of the inventive device, defined as the height of the device above the tissue surface, divided by the length of the device, is less than or equal to approximately 0.50, and more preferably approximately 0.10.
The height of the biasing spring is less than about 2 mm. In one particular embodiment, the biasing spring is formed to have a generally parabolic profile. The band preferably comprises a braided band, or, alternatively, a cable.
In one embodiment of the invention, the biasing spring comprises a first eyelet disposed in a center portion of the spring, for receiving the first end of the tensioning band, and a second eyelet disposed on an opposing side of the center portion of the spring, for receiving the second end of the tensioning band, wherein at least approximately four-fifths of the spring is disposed on either one side or the other of the first and second eyelets. More preferably, approximately two-fifths of the spring is disposed on one side of the first and second eyelets and approximately two-fifths of the spring is disposed on the other side of the first and second eyelets. The space efficiency of the biasing spring is at least about 50%, and preferably at least about 57%.
In another embodiment of the invention, the biasing spring comprises a first eyelet disposed on one edge of the spring, for receiving the first end of the tensioning band, and a second eyelet disposed on a second edge of the spring, for receiving the second end of the tensioning band, wherein substantially all of the biasing spring is disposed to one side of said eyelets.
The invention, together with additional features and advantages thereof, may best be understood by reference to the following description taken in conjunction with the accompanying illustrative drawings.
Referring now more particularly to the drawings, there is shown in
A dynamic compression device 12, which has been constructed in accordance with the principles of the present invention, is illustrated in a deployed orientation for holding the bone halves 16, 18 together. Also illustrated is a typical prior art dynamic compression device 14, also in a deployed configuration, for purposes of comparison. With reference also to
Now referring to
Both of the devices 12 and 14 are constructed of a suitable known medical grade material, preferably surgical stainless steel, to thereby yield similar performance characteristics which are necessary to supply dynamic compression to sternal halves 16, 18 so that optimum healing may occur. Sternal halves 16, 18 also represent a typical sternal cross-section in its width of approximately 24 mm.
The width of the sternum 10 ends up being a critical dimension in the procedure. The width of an adult sternum may range from 18 to 80 mm, but the tissue may not be dissected to access its entire width. While dissection may be done to accommodate larger devices, such trauma to tissue should be avoided. Thus, the figures show a sternal width of approximately 24 mm as this is the common dissected width used to accommodate the saw used for the initial osteomety.
At 24 mm in sternal width, the prior art device 14 is too large to function correctly. The suture 22 is unable to wrap around the bone appropriately, causing gaps 42 and 44. The gaps 42 and 44 cause the suture 22 to pull the device 14 directly into the sternal halves 16 and 18. This causes a rise in suture tension to realize the same compression between sternal halves 16 and 18, should gaps 42 and 44 not be present. The tension is such, in the system of device 14, that it is likely that arms 38 and 40 of the device will bend to the point of affecting the returning function of the spring 26. The net effect is that the device 14 cannot supply the same compression between the sternal halves 16 and 18 as is the case with the inventive device 12, even though the springs 26 and 24, respectively, have substantially the same spring constants and are fabricated of the same material. The width 29 of the prior art device 14 is twice the width 33 of the inventive device 12. The inventive device 12 also shows smaller gaps, with the band 20 lying on the bone surfaces 34, 36, enabling the band 20 to hold tension on both sides of the bone.
The dermal layer on top of the sternum is rather thin. Even when a surgeon employs only twisted wire to repair the sternum, some patients can feel that wire under their skin. Consequently, the profile of a closure device can have cosmetic as well as practical concerns. The dermal layer over the sternum on an average adult female is 5 to 10 mm thick. The prior art device 14 has a height 27 of approximately 5.3 mm (
The space efficiency of the device 12 is an important design criteria. A smaller, more efficient spring enables the device 12 to be used in more scenarios with less trauma to the patient. A material is capable of storing energy based on its volume. How that energy is stored and released is based on the length of the material and its cross-section. Both devices 12 and 14 have been designed to have equivalent performance both in energy stored and in the delivery of the energy. However, the respective space efficiencies of the springs of each device are far different. The space efficiency of the spring is defined as the total space it occupies divided by the space or volume the spring material actually physically occupies. In the case of the prior art device 14, the spring wire is 0.040 in. in diameter, and makes 7.5 revolutions. The spring itself is 0.210 in. in diameter and is 0.475 in. long. Thus, the space efficiency of the device 14 is the volume of the spring wire divided by the volume occupied by the spring, which equals 32%. Note that the end caps 50 and 48, and the arms 38 and 40 are left out of this calculation because they do not store energy. There is also some design space beneath the spring, between the bone and the spring that is not used and could be used by other designs. With this space included, the space efficiency of the device 14 drops to 28%.
The inventive device 12 more than doubles this space efficiency at 57%, by following a few innovative precepts. As can be seen in
Advantageously, the spring 24 as shown particularly in
While the inventive concept is disclosed as being particularly adapted for use in repairing the sternum after a thoracic cavity procedure, it is, of course, applicable to a great many other procedures requiring repair of bodily tissue, particularly bone.
Accordingly, although exemplary embodiments of the invention have been shown and described, it is to be understood that all the terms used herein are descriptive rather than limiting, and that many changes, modifications, and substitutions may be made by one having ordinary skill in the art without departing from the spirit and scope of the invention, which is to be limited only in accordance with the following claims.
This application claims the benefit under 35 U.S.C. 119(e) of the filing date of Provisional U.S. Application Ser. No. 61/037,582, entitled Dynamic Ring Compression Device, filed on Mar. 18, 2008, and expressly incorporated herein by reference, in its entirety. This application is also related to co-pending U.S. patent application Ser. No. 12/347,821, entitled Dynamic Suture Tensioning Device and filed on Dec. 31, 2008, and to U.S. Utility Patent Application Docket Nos. A-2313, entitled Knotless Dynamic Suture Tensioning Device and Methods, and A-2396, entitled Load Shaping for Dynamic Tensioning Mechanisms and Methods, both filed on even date herewith, all of which are commonly assigned and expressly incorporated herein, by reference, in their entirety.
Number | Date | Country | |
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61037582 | Mar 2008 | US |