Patent Application
20170172710
Traditional implant dentistry is typically a time-consuming and expensive process with multiple steps required over many weeks or months to scan the edentulous area for available bone, drill and place the implant, and allow for osseointegration and healing. Placement of the implant is particularly difficult for dental surgery professionals, as the location of available bone for drilling is often complicated to discern with traditional methods.
The key to success of cases using embodiments of the present implant system is maintaining the final prosthetic appliance in the proper position for placement. This is accomplished by a novel system in which the implant creation and placement is performed in reverse order. The prosthetic is created before any of the implants are placed. The prosthetic tells any dental surgeon exactly where to drill, so he is able to do so based solely on the final prosthetic appliance, bypassing the time-consuming and expensive steps necessary in traditional dental implant surgery. The patient can—in a matter of minutes—walk out of the dentist's office with teeth.
For the foregoing reasons, there is a need for a system that can inexpensively and quickly create a stent to be used in dental implant surgery without the complications associated with traditional implant dentistry. A stent is an appliance used during surgical procedures to provide a site for optimum implant placement.
The present invention is directed generally to a dental implant system and methods, and specifically to mini implant methods that reduce the need for the complications associated with traditional implant dentistry.
The model of the patient's mouth (“stone”) and the model of the stent are created using intraoral digital scanning. The word “stone” should not be restricted to any specific material, as the solid model could be made of many other materials. A computed tomography (CT) scan of the patient's edentulous and surrounding area are also obtained. These images are linked. Such oral CT scans—the digital scans as well as the linking—are well-known in the art to find available bone for implant placement. Once the CT scan has been performed, it is possible, and well-known in the art, to construct a surgical implant stent that would allow the dental surgeon to predetermine implant locations virtually, and surgically place them using computer added designing (CAD)/computer added machining (CAM) technology. In the first step of the dental implant system described herein, we are using traditional methods to virtually place the implants and then create the final prosthetic based upon the linked data from the CT scan, and the intraoral digital scan based on traditional CAD/CAM technology.
Two of the virtual implants have been created parallel and virtual analogues are added to the design of the edentulous space to be restored. The virtual analogues will go through the final prosthesis and extend beyond the device. This is then turned into a solid model (via 3d printing, for example) of the edentulous ridge with projecting parallel implant analogues.
The stent, i.e. the final prosthetic, is then placed and secured by the analogues and the model of the ridge. Onto this unit, a splint is created, encasing the stent/prosthesis, which fits firmly to the edentulous area of the stone. It sits directly on the mouth, on the precise spot on the arch where drilling is to occur. From here, everything is in place for the patient to receive a dental implant without the expense of time, energy, and money that traditional methods require. Only local anesthetic infiltration is necessary. Because the scan is created using a CT scan and CAD/CAM technology, the stent sits directly on the edentulous area. In some embodiments, the CAD/CAM methods of creating the analog and stone are accomplished by 3D printing.
An occlusal guard (“splint”) encases and supports the final prosthesis, assuring that it cannot move freely. It is necessary for the splint not to move freely, because it serves to secure the final prosthetic in place on the edentulous area of the mouth. The splint, with incorporated final prosthesis, can be secured with a stainless steel security pin placed through the lateral stent into holes pre-established into safe available bone. Usually surrounding teeth will be adequate support, and the pins will not be necessary. Access to the screw guide holes in the final restoration is maintained through the stent. In some embodiments, metal protective shields cross the stent over the final prosthesis on key locations to eventually act as separation guides. After implant placement, these protective shields show the dentist where to safely cut the stent in order to release the final prosthesis from the stent. If support pins had been used, they are now removed, and the pieces of the stent are removed and discarded, leaving the prosthesis in place as a permanent restoration.
These and other features, aspects, and advantages of the present invention will become better understood with regard to the following description, appended claims, and accompanying drawings. It is to be understood that the foregoing summary addresses only a few exemplary aspects of the invention, and that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention as claimed.
Taking a CT scan of a patient's edentulous and surrounding area is well-known in the dental arts, as is the ability to develop first a laboratory model, and then a physical model of the arch, analog, and stent 12, using CAD/CAM technology. A major innovation of the present invention is the single article of manufacture which comprises an acrylic splint 12 made on the model, already supporting the final prosthesis 10. The splint 12 encases the final prosthesis 10, assuring that it cannot move freely.
Once the stent 12 is in final position on the patient, in some embodiments, single implants will be used to replace anterior and pre-molar teeth of 3 mm diameter. In some embodiments, two, 2 mm implants will be used for each molar replacement (preferably distal and mesiolingual).
The active (cutting) section 16 of the final prosthesis 10 can be, for example, from 8 mm to 16 mm in length. Above this is the 3 mm gingival collar 18. Above this segment is the 5 mm segment 20 with deeper threads that engage the final restoration. In some embodiments, the 5 mm segment 20 will have no threads, but will be smooth. Finally is the implant head 24 which is also 5 mm in height and has a hollowed 4 mm deep internal hex pattern to accept the torque driver 26.
In some embodiments, the tip of the active section 16 of the implants will be covered with a 5 mm nylon sleeve, which does not touch the conical point of the tip as it narrows. This sleeve will be used as a drill guide for the implant, ensuring that it is introduced into the prosthetic/stent with the proper inclination. The implant will act as a screw to hold the prosthetic, and the splint encases the prosthetic. The sleeve then stays in place as the implant advances into bone. After drilling, the sleeve acts as a stop for the head of the implant. The sleeve advances with the implant until it rests on a ledge/platform which halts its forward movement as the implant proceeds into the bone, and then stops progression of the implant when the implant head rests on the sleeve's superior segment.
This equates to single piece implants measuring, for example, between 21 mm and 29 mm. All measurements in the preceding paragraphs are by way of example only, and are not restrictive of the invention as claimed.
In the invention described herein, two of the implants must be parallel, and the others divergent, in order to prevent the splint from moving freely, securing the implants in place. The stent/prosthetic are kept in place by the splint as the implant advances into the bone.
In the foregoing description, various features are grouped together in a single embodiment for purposes of streamlining the disclosure. This method of disclosure is not to be interpreted as reflecting an intention that the claimed invention requires more features than are expressly recited in each claim. Rather, as the following claims reflect, inventive aspects lie in less than all features of a single foregoing disclosed embodiment. Thus, the following claims are hereby incorporated into this description, with each claim standing on its own as a separate embodiment of the invention.
Although the present invention has been described in considerable detail with reference to certain preferred versions thereof, other versions are possible. Therefore, the spirit and scope of the appended claims should not be limited to the description of the preferred versions contained therein.
This patent application depends for priority on Provisional Application 62/094,617 filed on Dec. 19, 2014. This application is incorporated herein by reference, but is not admitted to be prior art with respect to the present invention by its mention in the background.
