1. The Field of the Invention
This invention relates to mechanical fasteners for surgical use and, more particularly, to half pin fasteners for bone fixators.
2. The Relevant Technology
Standard half pins are employed for the fixation of long bones that have been fractured or surgically divided. Half pins are typically non-cannulated and are threaded to engage both sides of the bone and prevent slippage. Typically, a hole must first be drilled in the bone. Then, the drill bit is removed and the half pin inserted.
Problems associated with this method of application include dull drill bits, heat generation (burned bone), eccentric pin placement and multiple steps involved in the insertion of each pin. As a result, surgical time and radiographic imaging exposure are increased and secure fixator placement may be compromised. Suboptimal pin placement may result in pin loosening, pin breakage, stress fracture of the bone, or bone fragmentation (i.e., ring sequestrum), therefore ultimately requiring secondary surgery.
External frames (fixators) are ubiquitous in the orthopedic armamentarium for managing long bone fractures and/or for limb lengthening or deformity correction. The frames are attached to long bone(s) via multiple half pins that are inserted percutaneously (i.e., blindly) into bone segments. Central and concentric pin placement requires skill and intuition and is usually documented by fluoroscopy. Frames are typically worn for weeks, months or in some instances, more than a year. The outcome of this treatment technique is predicated upon secure and accurate frame attachment and is reliant upon optimization of the pin-bone interface. Eccentric pin placement causes pin related problems including drainage and infection. Consequently, bending or breakage of pins is relatively common, thereby complicating this method of treatment.
A variety of orthopedic half pins are available on the market. While some are tapered or self-tapping, all require pre-drilling of the bone prior to pin insertion. A common pitfall of drilling bone, exacerbated by dull drill bits, is the potential to drill eccentric holes, compromising the integrity of the bone and the strength of fixation. This is often unrecognized until later when the bone/pin interface fails due to, for instance, dead bone (heat necrosis), secondary infection, pin fatigue, or stress fracture of the bone. These situations typically mandate secondary, unplanned surgical intervention to revise pin placement and alter the frame construct. Such unanticipated steps in fracture management or deformity correction may comprise the outcome of the surgery.
What is needed is a fastener that overcomes these limitations in a product which minimizes surgical time and radiographic image exposure, while providing a reliable, accurate and secure placement of the half pin fastener. Such a fastener should also lend itself to use with most makes and models of fixators.
In one embodiment, a drill-pin implant, which meets the needs identified above, has an elongated, cylindrical body extending along a central axis. The cylindrical body has opposing end portions, namely an operative end portion or tip and a tool engaging portion or application end. The operative end portion is formed so as to be suitable for penetrating bone. The tool engaging end portion is formed so as to be suitable for engagement with a hand or power drill. The body is cannulated through its entire length to permit drill-pin insertion over a guide pin. The body further has an external threaded portion suitable for engaging with the bone, in order to prevent the implant from slipping. The thin, unobtrusive guide pin is first inserted into the bone, documenting precise and concentric placement with radiographic imaging. The drill-pin implant is inserted over the guide pin and advanced until the drill tip penetrates the far side of the bone and the external threads engage the near side. The guide pin is then removed. A bone plate or fixator may then be affixed to the implant, as appropriate, and the incision closed.
The inventive drill-pin implant and related system ensures efficient and accurate placement of bone implants.
In an advantage of the invention, the drill is “disposable” (in that it is for single use), it is always sharp and of known true diameter, thus reducing the likelihood of intraoperative or postoperative complications such as burned bone or stress fractures.
In a further advantage the drill-pin serves as the implant, thus saving the cost of stocking and sharpening multiple drill bits and carrying an expanded inventory of pins.
Various embodiments of the present invention will now be discussed with reference to the appended drawings. It is appreciated that these drawings depict only typical embodiments of the invention and are therefore not to be considered limiting of its scope.
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Further, the diameter of the drill-pin implant 30 may be stair-stepped or relieved (not shown) so as to provide clearance after the operative end 36 penetrates a near wall 52 (
Drill-pin implant 30 is cannulated to enable precise and concentric implant or pin placement over the guide pin 44 which is then removed. The single use and disposable drill-pin implant 30 features a short cutting flute 54 to avoid damage to soft tissue (e.g., skin 56 and muscle 60 shown in
One embodiment of a drill-pin system 62 (
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In alternative embodiments where guide pin 44 has a cutting surface formed on the end thereof, such as cutting flutes 64 in
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In one alternative method as discussed below with regard to
In a fourth step 82, the location of drill-pin implant 30 is optionally confirmed fluoroscopically. Alternatively, the position of guide pin 44 can be confirmed fluoroscopically before insertion of drill-pin implant 30.
In a fifth step 84, the guide pin 44 is removed. In an optional sixth step 86, steps (i) to (vi) are repeated until the desired number of drill-pin implants 30 are located. In this case, each subsequent drill-pin implant 30 (average three per bone segment) is inserted in an identical fashion. In an optional seventh step 90, the drill-pin implant or implants 30 are then connected to an external fixator, and, where necessary, any excess portions of the drill-pin implants are cut off. In a final step, the incision may now be closed.
Depicted in
Each tooth 116 has a planar front face 118 that terminates at an outside cutting edge 120, a top surface 122 that slopes back toward second end 110, and a back face 124 that is beveled so as to expose the planer front face 118 of the next adjacent tooth 116. Formed between each cutting tooth 116 in alignment with each front face 118 is an elongated channel 128 that is recessed into body 102. In the depicted embodiment, each channel 118 is linear and extends longitudinally along body 102. In alternative embodiments, channels 118 can also be curved. In part, channels 118 provide a path through which the bone matter cut by teeth 116 can be removed from the tunnel being bored.
It is appreciated that cutting teeth 116 can have a variety of different configurations and can be replaced with a variety of other types of cutting surfaces that can be used to bore drill-pin implant 100 into bone 12. Cutting teeth 116, however, have been found to be uniquely beneficial when it is desired to mount drill-pin implant 100 at an angle other than normal to the longitudinal axis of the bone. That is, it has been found that unique benefits can be achieved by mounting drill-pin implants 100 into bone so that an inside angle is formed between the longitudinal axis of drill-pin implant 100 and the longitudinal axis of bone 12 that is less then 90° and more commonly between about 15° to about 75° with about 30° to about 60° being more common. Conventional fluted drill bits traditionally have poor initial engagement when drilling at an oblique angle. As such, conventional fluted drill bits can cause relative slow drilling, increased heating of the bone, and potential walking of drill bit. Cutting teeth 116, however, have excellent engagement with a cutting surface when oriented at an oblique angle relative to the surface. As such, use of cutting teeth 116 decreases cutting time while minimizing heat transfer and any potential for walking.
External threads 130 radially outwardly project from exterior surface 106 of body 102 so as to encircle body 102 in a helical pattern. External threads 130 can comprise one or more threads and can have a variety of different pitches. An enlarged view of one embodiment of external threads 130 is shown in
If desired, external threads 130 can extend to second end 110. In the depicted embodiment, however, external threads 130 extend along a section of body 102 at a location spaced apart from both opposing ends 108 and 110. A proximal section 132 of body 102 has a smooth, substantially cylindrical configuration extending from external threads 130 to second end 110. The drill-pin implants of the present invention are typically made of metal, such as such as titanium or stainless steel, but other suitable materials can also be used.
As previously mentioned, drill-pin implant 100 can be used in association with guide pin 44 or a variation thereof in the same manner as discussed with regard to drill-pin implant 30. Furthermore, the various drill-pin implants of the present invention can also be used in association with a tubular drill sleeve. For example, depicted in
During use, drill sleeve 140 is initially passed over drill-pin implant 100 so as to cover external threads 130 as drill-pin implant 100 is passed through the soft tissue so as to engage against bone 12. This placement can occur concurrently with or subsequent to positioning guide pin 44 into bone 12. Alternatively, drill sleeve 140 can be positioned over drill-pin implant 100 after drill-pin implant 100 is passed over guide pin 44 but prior to rotation of drill-pin implant 100. Drill sleeve 140 functions as a cover for external threads 130 so that external threads 130 do not directly engage the surrounding soft tissue and potentially tear or damage the soft tissue as drill-pin implant 100 is rotated. After drill-pin implant 100 is securely positioned, sleeve 140 can be removed and discarded or sterilized for reuse.
The inventive drill-pin implants, systems, and methods of the present invention have a number of benefits. For example, the drill-pin implants, guide pins, and/or guide tubes can be designed to be disposable after a single use. As a result, the drill-pin implants are always sharp for drilling, have a known true diameter, and no subsequent sterilization is required.
Furthermore, because the drill-pin implant serves as both the drill and the pin, the cost for purchasing and stocking separate drill bits with their related sharpening and sterilization is eliminated. In addition, carrying an expanded inventory of pins is limited.
By use of the narrow guide pin, the guide pins can be more accurately positioned, thereby avoiding the common problems of walking of the larger drill bits, excessive heating of the bone (e.g., heat necrosis), and eccentric placement of the implants (e.g., high stresses promoting bone fracture).
The inventive system also provides an easier and faster method of implanting the drill-pin implants. Specifically, because the drill bit and pin can be combined in the inventive implants, the inventive method avoids multiple passes of instruments and implants through the skin and muscle. In particular, a separate drilling step may be avoided. In addition, in conventional methods it can be difficult to locate the drilled hole after the drill bit is removed. The present invention has no such problem. The inventive implants can also be used with external fixators (frames) that are commonly employed for the stabilization of long bones during fracture management or deformity correction.
In another advantage, radiographic exposure (e.g., fluoroscopy) is reduced because once the guide pin placement is verified; the only additional documentation required is the depth of drill-pin insertion.
In another advantage, the drill-pin implants may be provided in standard lengths as the excess is easily cut off. Thus, a large variety of half pin lengths and diameters is no longer required.
Multiple variations and modifications are possible in the embodiments of the invention described here. Although certain illustrative embodiments of the invention have been shown and described here, a wide range of modifications, changes, and substitutions is contemplated in the foregoing disclosure. In some instances, some features of the present invention may be employed without a corresponding use of the other features. Accordingly, it is appropriate that the foregoing description be construed broadly and understood as being given by way of illustration and example only, the spirit and scope of the invention being limited only by the appended claims.
The present application is a continuation-in-part of International Application No. PCT/IB2004/000429, Filed Feb. 20, 2004 which claims priority to U.S. Provisional Application No. 60/449,327, filed Feb. 22, 2003.
Number | Date | Country | |
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60449327 | Feb 2003 | US |
Number | Date | Country | |
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Parent | PCT/IB04/00429 | Feb 2004 | US |
Child | 11198637 | Aug 2005 | US |