The present disclosure generally relates to apparatuses and methods for anesthetizing a dental patient during dental procedures such as a root canal. Oftentimes it is necessary to administer an anesthetic to the tooth being treated for the comfort of the dental patient. Delivering the anesthetic directly into the jaw bone of a patient, called intraosseous injection, is quick and highly effective but can have a relatively short duration. In addition, a dental dam is often placed over the tooth being treated in order to control the environment. The apparatuses and methods disclosed herein permit intraosseous injection of an anesthetic into the jaw bone of the dental patient multiple times without removing or disturbing the dental dam.
As background, dental providers such as dentists and endodontists typically administer a local anesthetic, such as articaine or lidocaine, to dental patients for the duration of most dental procedures. The local anesthetic numbs the tooth subject to the dental procedure and permits the dental patient to have a relatively pain-free experience. The local anesthetic may be delivered to the dental patient in several ways, including but not limited to inferior alveolar nerve block (IANB), buccal infiltration, and intraosseous injection. The first two techniques primarily inject the anesthetic into the soft tissue around the tooth, and they have the advantage that they are relatively easy to administer and a single injection is effective for most patients. However, there are several disadvantages to IANB and buccal infiltration. First, the anesthetic can require a relatively long time to take effect, and, in some patients, a second injection must be given to fully numb the patient. Second, the duration of the anesthetic's effect can be somewhat short, requiring the anesthetic to be administered a second or third time during the procedure. Finally, these techniques may also have a lower success rate on some patients, which may require a supplemental injection of anesthetic to fully numb the patient.
The intraosseous injection technique injects the anesthetic directly into the jaw bone of the dental patient. This technique has the advantage that it may take effect very quickly and may generally have a higher rate of success over a wide range of patients having various dental maladies. However, administering the anesthetic in this manner is more complicated, as the provider must drill a hole into the patient's jaw bone in order to gain access to the cancellous portion of the jaw bone. This is typically accomplished using a hollow drill bit which leaves behind a cannula or sleeve embedded into the jaw bone through which the anesthetic may be delivered. As an example, the X-Tip® Drill and Guide Sleeve from Dentsply® Maillefer® (Ballaigues, Switzerland) may be used to drill a hole in the jaw bone of the patient in order to anesthetize dental patients via intraosseous injection. As another example, the Stabident system from Fairfax Dental, Inc., (Miami, Fla.) may also be used to gain access to the cancellous portion of the jaw bone. However, for this method the duration of the anesthetic's effect may be relatively short; and in some instances, the provider may need to administer the anesthetic a second time or third time in order to maintain the comfort of the patient.
Furthermore, for some dental procedures, the provider may place a “dental dam” over the tooth (or teeth) subject to the procedure. The dental dam may isolate the tooth from the rest of the mouth and may prevent the patient's saliva from interfering with the dental procedure, which could potentially contaminate the tooth with microorganisms, possibly leading to a post-procedural infection. In addition, the dental dam may prevent dental instruments and/or other dental materials from coming into contact with the patient, which may cause discomfort to the patient or may increase the risk of the patient accidentally swallowing such items. The dental dam usually blankets the tooth in a manner which causes the injection site for the anesthetic to be covered up. The dental dam may be constructed of latex or nitrile, and it may be installed by the provider at the beginning of the dental procedure.
In cases where a dental dam is used and a re-administration of the anesthetic to the patient is necessary, the provider may be required locate the original intraosseous injection site underneath the dental dam. Depending on the location of the injection site in relation to objects such as the dental dam, clamps, and so forth, access may be quite challenging. Temporary removal of the dental dam may at times be the best option to properly access the intraosseous injection site. This can cause frustration for the provider, discomfort for the patient, and will likely extend the procedure time.
Accordingly, a solution is needed for dental procedures which use a dental dam, and which require multiple administrations of the anesthetic. The apparatuses and methods disclosed herein overcome the potential inherent time duration disadvantage in intraosseous injection for dental procedures using a dental dam by allowing the provider to deliver the anesthetic multiple times to the patient without the provider having to remove or disturb the dental dam.
Limitations in the prior art will become apparent to those skilled in the art after reviewing the specification below and the corresponding drawings.
In one embodiment, an apparatus for delivering an anesthetic into a jaw bone of a dental patient is disclosed. The apparatus comprises a flexible tube having a first end and a second end, a needle, and a coupler, wherein: the first end of the flexible tube is configured to be fluidly coupled to a delivery system capable of injecting the anesthetic into the flexible tube; the second end of the flexible tube is fluidly coupled to the needle such that the needle is at substantially a right angle to the second end of the flexible tube; the needle is configured to be inserted into a proximal end of a cannula and, when inserted, is capable of delivering the anesthetic from the flexible tube into the cannula; the coupler is disposed at the second end of the flexible tube, surrounds a portion of the needle, and is configured to be removably affixed to the proximal end of the cannula, wherein: when the coupler is affixed to the proximal end of the cannula, the coupler is configured to fluidly seal the second end of the flexible tube to the cannula; and when a distal end of the cannula is inserted into the jaw bone of the dental patient, the needle is inserted into the proximal end of the cannula, the coupler is affixed to the proximal end of the cannula, and the delivery system is fluidly coupled to the first end of the flexible tube, the delivery system is capable of delivering the anesthetic through the flexible tube, the needle, and the cannula into the jaw bone of the dental patient one or more times.
In another embodiment, an apparatus for delivering an anesthetic into a jaw bone of a dental patient is disclosed. This apparatus comprises a delivery system, a flexible tube having a first end and a second end, a needle, a coupler, and a cannula having a proximal end and a distal end, wherein: the first end of the flexible tube is configured to be fluidly coupled to the delivery system capable of injecting the anesthetic into the flexible tube; the second end of the flexible tube is fluidly coupled to the needle such that the needle is at substantially a right angle to the second end of the flexible tube; the needle is configured to be inserted into the proximal end of the cannula and, when inserted, is capable of delivering anesthetic from the flexible tube into the cannula; the coupler is disposed at the second end of the flexible tube, surrounds a portion of the needle, and is configured to be removably affixed to the proximal end of the cannula, wherein: when the coupler is affixed to the proximal end of the cannula, the coupler is configured to fluidly seal the second end of the flexible tube to the cannula; and when the distal end of the cannula is inserted into the jaw bone of the dental patient, the needle is inserted into the proximal end of the cannula, the coupler is affixed to the proximal end of the cannula, and the delivery system is fluidly coupled to the first end of the flexible tube, the delivery system is capable of delivering the anesthetic through the flexible tube, the needle, and the cannula into the jaw bone of the dental patient one or more times.
In yet another embodiment, a method is disclosed for delivering an anesthetic into a jaw bone of a dental patient. The method comprises: fluidly coupling a delivery system to a first end of a flexible tube; inserting a distal end of a cannula into the jaw bone of the dental patient in a manner that allows the dental patient to be anesthetized; fluidly coupling a second end of a flexible tube onto a proximal end of the cannula, wherein the second end of the flexible tube is configured to be at a substantially right angle to the cannula; and delivering the anesthetic from the delivery system through the flexible tube, the needle, and the cannula, and into the jaw bone of the dental patient one or more times.
The embodiments set forth in the drawings are illustrative and exemplary in nature and not intended to limit the inventions defined by the claims. The following detailed description of the illustrative embodiments can be understood when read in conjunction with the following drawings, where like structure is indicated with like reference characters and in which:
As used herein, the word “provider” is defined to be dentists, dental assistants, nurses, nurse practitioners, endodontists, and so forth. Although “provider” may indicate a single individual, it is also intended to signify two or more people acting in concert or one or more people acting under the direction of another. Also, as used herein, the phrase “jaw bone” is defined to be either the lower jaw bone (often referred to as the “jawbone,” “mandible,” or “lower jaw”) or the upper jaw bone (often referred to as the “maxilla”).
The flexible tube 12 may be constructed of any suitable material capable of delivering anesthetic to the dental patient. For example, nylon may be used to construct the flexible tube 12. Also, the flexible tube 12 may of sufficient length to allow the delivery system for anesthetic to be place at a convenient location near the dental patient. Also, the flexible tube 12 may be clear or opaque in order to permit the provider to observe whether the anesthetic is present therein.
In
The distal end 20B of the cannula 20 may be inserted into the jaw bone of the dental patient such that the anesthetic 18 is capable of being delivered to the dental patient through the flexible tube 12, needle 14, and cannula 20. The second end 12B of the flexible tube 12 may be configured in a manner that it neither interferes or obstructs the provider, or causes discomfort for the patient; and the flexible tube 12 may be routed in a way that doesn't disturb a dental dam placed in the patient's mouth. For example, the flexible tube 12 may be routed in a manner so that it parallels in inside of the patient's cheek before exiting the mouth of the patient. The first end 12A of the flexible tube 12 may be configured to be fluidly coupled to the delivery system for the anesthetic 18 such that the delivery system is capable of delivering the anesthetic 18 through the flexible tube 12, needle 14, and cannula 20 into the jaw bone of the dental patient one or more times.
When the second end 12B of the flexible tube 12 is fluidly coupled to the proximal end 20A of the cannula 20, the male friction lock 20C is inserted into the female friction lock 16A such that sufficient friction between them prevents the coupler 16 from becoming fluidly uncoupled from the proximal end 20A of the cannula 20 when the anesthetic 18 is delivered into the jaw bone, typically under a relatively low fluid pressure. However, this friction may be low enough so that the provider is still able to manually remove the coupler 16 from the proximal end 20A when desired. Other techniques of fluidly coupling the coupler 16 to the proximal end 20A of the cannula 20 may be used as well, including those known now in the art and those which may be developed in the future. The needle 14 may be construction of stainless steel, a metal alloy, or any other suitable material. As discussed above, the needle 14 may be designed so that it may be inserted into the hollow proximal end 20A of the cannula 20 when the cannula 20 and coupler 16 are fluidly coupled.
Continuing to refer to
Other techniques for fluidly coupling the first end 12A of the flexible tube 12 to the delivery system 32A are also contemplated. For example, a self-tapping screw may be used which may screw into the delivery system 32A. The self-tapping screw may have a thin needle contained within it in order to puncture the membrane of a cartridge containing the anesthetic. The membrane and cartridge may be part of the delivery system 32A for the anesthetic, and this arrangement may allow the dental provider to easily and quickly fluidly couple the first end 12A of the flexible tube 12 to the delivery system 32A for the anesthetic.
In addition to the apparatuses shown and described herein, methods are also disclosed for anesthetizing dental patients. In one embodiment, a method is disclosed for delivering an anesthetic to a dental patient, the method comprising: fluidly coupling a delivery system for the anesthetic to a first end of a flexible tube; inserting a distal end of a cannula into the jaw bone of the dental patient in a manner that allows the dental patient to be anesthetized; fluidly coupling a second end of a flexible tube onto a distal end of the cannula, wherein the second end of the flexible tube is configured to be at a substantially right angle to the cannula; and delivering the anesthetic from the delivery system through the flexible tube, the needle, and the cannula, and into the jaw bone of the dental patient one or more times.
While particular embodiments and aspects of the present invention have been illustrated and described herein, various other changes and modifications may be made without departing from the spirit and scope of the invention. Moreover, although various inventive aspects have been described herein, such aspects need not be utilized in combination. It is therefore intended that the appended claims cover all such changes and modifications that are within the scope of this invention.
This application claims the benefit of provisional application Ser. No. 62/923,569, filed Oct. 20, 2019, the disclosure of which is incorporated herein by reference.
Number | Date | Country | |
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62923569 | Oct 2019 | US |