Dental implants of the character receivable within a bore provided in the jawbone are old in the art. Typically such implants comprise an apertured body portion which is placed within a bore drilled in the bone. The body portion is typically designed so that during a period of several months after its emplacement within the bore, bone tissue will grow into the aperture so as to secure the body portion of the implant in place within the bone bore. At some point in the treatment, an artificial tooth or other prosthetic component is secured to the body portion.
These procedures are undesirable in several respects. In the first place, the procedure is protracted and requires multiple visits to the oral surgeon. Secondly, during the extended period of time required for the bone tissue to grow into and around the implant, the patient can have an uncomfortable and unsightly cavity where the prosthetic component, such as an artificial tooth, will eventually go. Additionally, these procedures do not always provide adequate anchoring of the implant to the jawbone so that in time the implant can loosen, requiring further remedial work or an alternative procedure.
Several types of implants using mechanical locking means for securing the 2530 implant in place within the bore in the jawbone have been developed. Exemplary of such devices is the device described in U.S. Pat. No. 3,708,883 issued to Flander. Other dental implants are illustrated and described in U.S. Pat. Nos. 5,004,421, 5,087,199 and 6,142,782 issued to Lazarof. The Lazarof dental implant makes use of mechanical securement means, but unlike the Flander device, the Lazarof device includes means by which selected dental prosthetics of standard design can be threadably interconnected. In this way, angular corrections of the prosthetic, such as an artificial tooth, can readily be made.
Further, in one form, these prior Lazarof implants are positively secured within the bore in the bone by two separate but cooperating securement mechanisms. The first securement mechanism comprises self-tapping, external threads provided on the tubular body of the device which are threaded into the bone by rotating the device in a first direction. The second cooperating securement mechanism comprises a plurality of bone penetrating anchor blades formed on the skirt portion of the tubular body which are moved into a bone engagement position only after the implant has been securely threaded into the bone. The anchor blades are moved into the bone engagement configuration by rotating a threaded expander member also in a first direction. However, because the threads on the expander member are opposite to the threads on the tubular body, rotational forces exerted on the expander member continuously urge the implant in a tightening direction. In other words, as the anchor blades are urged outwardly, the implant is continuously urged into threaded engagement with the bone. This double locking approach permits the selected prosthetic component to be connected to the implant immediately.
The present invention provides even greater implant security than the prior art. When a tooth is extracted from a patient's mouth, the resulting cavity has a natural tapered shape. The cavity will be wider at the gumline proximal to the cavity opening. Prior art does not account for this natural tapered shape. In contrast to the prior art, the instant invention has an upper tapered hood as well as an expandable skirt. The stability of the implant is improved and abutment and prosthetic options are increased. This invention is called a bipolar implant.
The present invention is an implant that compacts bone bi-directionally, resulting in an improved, more stable implant. The natural configuration of the cavity of an extracted tooth tapers and expands outwardly towards the gümline. The invention improves the stability of the implant and addresses the configuration of a natural cavity after tooth removal.
In the preferred embodiment of the invention, the implant assembly has a hood 15 that tapers outward, in the direction of the oral cavity of the patient's mouth. Adjacent to the hood, is a tapered, tubular body that includes a skirt receivable within a bore provided in the bone of a patient. Within the tubular body is a draw screw which has a head which is captured within the hollow body, and a threaded shank which is connected to the draw screw head and extends to an end of the skirt. The draw screw head engages an internal shoulder contained within the tapered hollow body to form a seal which isolates a first hollow body chamber on one side of the draw screw head from a second hollow body chamber on an opposite side thereof. An expansion nut has an inner threaded cavity into which the shank of the draw screw is threaded. Rotation of the draw screw through the inner cavity of the expansion nut causes radial movement of the skirt from a first retracted position to a second expanded position.
In an alternative embodiment of the invention the hood has a portion removed so that the resulting circumference around the hood is non-circular.
In another embodiment of the invention, the hood is adjacent to beveled coronal rings, which are attached to an upper collar.
In another embodiment of the invention, the hood is adjacent to an upper collar, said collar having a circumference that is equal to the largest circumference of the hood.
In an alternative embodiment of the invention, the abutment is permanantly integrated into the upper hex portion of the implant by machining, eliminating the need for attaching a separate abutment.
The accompanying drawings illustrate the invention. In such drawings:
As shown in the drawings for purposes of illustration, the present invention is concerned with a dental implant. It will be understood, however, that the present invention may be applied to various types of implantable prosthetic devices, and is not limited to dental implants.
With reference to
Adjacent to the lower hood 19 is a tubular body 3. The tubular body 3 tapers outward towards the hood 1. The outside surface of the tubular body has bone engaging protrusions 24 which carve into the bone of the patient's jaw. The tubular body ends at the lower hood 19. The tubular body 3 is provided with internal threads 5 which are adapted to threadably receive an abutment 6.
Next to the tubular body 3 is a skirt portion 2 radially movable from a first 155 retracted position to a second expanded position. To move the skirt portion 2 into the second expanded position, there is provided an expander means shown in the drawings as comprising an expansion nut 4 and a draw screw 8. As shown in
Referring to
Importantly, the draw screw 8 is configured to sealingly engage the internal shoulder 13 of the tapered tubular body 3 to isolate a first hollow body chamber 15 (defined as the area within the tubular body 3 beneath the shoulder 13 into which the threaded shank 7 extends), from a second hollow body chamber 16 (defined as the interior of the tapered hollow body 3 above the internal shoulder 13), shown in
As most clearly shown in
Prior to placing the implant assembly 18 within the jawbone of a patient, the implant assembly 18 is prepared by simply placing the draw screw 8 within the tubular body 3 so that the head 84 of the draw screw 8 rests against the internal shoulder 13. The expansion nut 4 is threaded onto the bottom end of the threaded shank 7 just enough to ensure that the tabs 10 of the expansion nut 4 will be properly aligned with the tapered slits 17. This assembly of the tubular body 3, the draw screw 8 and the expansion nut 4 is then placed within the bore. A screwdriver or allen wrench may be inserted through the upper end of the tubular body 3 to turn the draw screw 8 for the purpose of drawing the expansion nut 4 upwardly into the tubular body 3. If necessary, a wrench may be utilized to engage the upper hex 9 to prevent rotation of the tubular body 3. The tabs 10 ensure that the expansion nut 4 does not rotate relative to the tubular body 3. As the expansion nut 4 is drawn into the tubular body 3, the bone anchor segments 11 expand outwardly so that the penetrating protuberances 12 slice into the bone in a manner to securely lock the tubular body 3 within the bore of a patient's mouth.
This application is a conversion of provisional application 60/415,830, pursuant to 35 U.S.C. 111(b)(5).
Number | Date | Country | |
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60415830 | Oct 2002 | US |