BITE BLOCK
20220134036 ยท 2022-05-05
Inventors
Cpc classification
A61M16/0493
HUMAN NECESSITIES
International classification
Abstract
Disclosed herein are systems, designs, and methods for a bite block and for using a bite block or surgical mouth guard. The bite block can accept various tubes used during intubation. The bite block also provides passage that allows a patient to be intubated or to breath while using a bite block. The bite block may also mitigate migration of tubes used during intubation.
Claims
1. A bite block formed to protect the teach when used a medical procedure comprising: a U-shaped member, the U-shaped member comprising: a top surface a bottom surface opposite the top; a first end; a second end; a first leg; a second leg; a middle section, wherein the middle section is between the first and second legs; a central cutout in the middle section; and at least one or more side apertures.
2. The bite block of claim 1, wherein the first leg and the second leg include at least one side aperture configured to receive a tube or medical instrument.
3. The bite block of claim 1, wherein the first leg and second leg are separable from the middle section.
4. The bite block of claim 1 further comprising separable popout sections disposed within the first aperture, the second aperture, and the center cutout.
5. The bite block of claim 2, wherein the side aperture opens to the bottom surface of the bite block to create an opening slot.
6. The bite block of claim 2, wherein the side aperture opens to the top surface of the bite block to create an opening slot.
7. The bite block of claim 1, wherein the bite block further includes a trough or channel on the top surface to accommodate placement of the user's teeth.
8. The bite block of claim 1, wherein the bite block further includes grip mechanisms that can include indica, ridges or the combination thereof to create a hold on the user's teeth.
9. The bite block of claim 8, wherein the grip mechanism is composed of a pliable material that is softer than the material formed to create the body of the bite block.
10. The bite block of claim 1, wherein the bite block is formed from a single piece of material.
11. The bite block of claim 1, wherein the bite block is formed from more than one piece of material.
12. The bite block of claim 1, wherein the first leg and the second leg have a thinner height than the middle section to create a wedge shaped configuration for the bite block.
13. The bite block of claim 1, wherein the first leg and second leg include score lines to allow for accommodation to various sizes.
14. The bite block of claim 1, wherein the bite bock further includes a strap mechanism to hold the bite block in place.
15. A method of using the bite block comprising: placing the bite block in a patient's mouth; wherein the bite block includes a U-shaped member comprised of a top surface, a bottom surface, a first end, a second end, a first leg configured with a side aperture, a second leg configured with a side aperture, and a middle section, wherein the middle section includes a central cutout configured to receive an intubation tube, inserting at least one tube into the patient's mouth; placing the at least one tube in communication with the central cutout configured to receive the intubation tube in the bite block.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
[0023] As required, detailed embodiments of the present invention are disclosed herein; however, it is to be understood that the disclosed embodiments are merely exemplary of the invention, which may be embodied in various forms. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a basis for the claims and as a representative basis for teaching one skilled in the art to variously employ the present invention in virtually any appropriately detailed structure.
[0024] Referring now to
[0025] As shown in
[0026] The top surface 10 of the bite block 1 may be smooth. In other embodiments the top surface 10 may be rough to prevent the bite block 1 from slipping while in the mouth of the patient. The top surface 10 may also have a trough to accommodate the teeth or gums of a patient. In a further embodiment, the top surface may be configured to receive a material to help in holding the user's teeth in place. The material can be a reusable sticky or tacky material or any similar material that is pliable and allows for forming around and in communication with the teeth of a patient. The material will still allow the bite block to be removed but can engage the teeth of the patient. In a further embodiment the top surface may have indicia or raised members 15 to create surface area that communicates with a user's teeth. Similarly, the bottom surface 20 of the bite block 1 may be smooth. In another embodiment, the top surface 10 and the bottom surface 20 can include any means known in the industry to create traction between the bite block and a user's teeth such as may have ridges to prevent the bite block 1 from slipping while in a patient's mouth. In other embodiments the bottom surface 20 may be rough to prevent the bite block 1 from slipping while in the mouth of the patient. The bottom surface 20 may also have a trough or indentions to accommodate the teeth or gums of a patient. In an additional embodiment the top surface 10 and the bottom surface 20 may be formed from a soft material which allows the bite block 1 to accommodate a patient's teeth. In this regard, the top surface 10 and the bottom surface 20 may be softer than the other parts of the bite block 1. The top surface 10 and the bottom surface 20 may have indicia or raised members 15 for assisting in placement of the bite block 1. The indicia may also provide friction or roughness for preventing the bite block 1 from slipping out of a patient's mouth and can be composed of material that is softer or tacky or sticky to create the connection with the patient's teeth.
[0027] The bite block 1 may have a wedge like shape where the section of the bite block 1 nearest the first end 5A and second end 5B is thinner than the middle section 70. In this regard, the bite block 70 may have dimensions that allow the bite block 1 to fit in the mouth of a patient. One of skill in the art will appreciate that the middle section 70 of the bite block 1 may have the same thickness or be thinner than the first or second ends 5A and 5B. In an alternative embodiment the bite block 1 may have varying widths to allow for the placement in the mouth of a patient.
[0028] As shown in
[0029] The middle section 70 of the bite block 1 may also have a first side aperture 60A and a second side aperture 60B that open relative to the bottom surface 20 to create an opening slot. The first and second side apertures may be on each side of the middle cutout 50. As shown in
[0030] In an additional embodiment each side aperture 60A and 60B may have a separable popout section disposed within the side aperture. The center cutout 50 may also have a separable popout section disposed within the center cutout 50. The separable popouts provide the user the ability to determine the number or size of apertures needed for a procedure. A user may remove the popout sections according to the desired aperture configuration. In this regard, the bite block 1 can have various numbers of popouts for a desired configuration and is therefore customizable by the medical personal for use with the desired procedure.
[0031] The bite block 1 can also include a configuration that allows for the acceptance of a strap or other holding mechanism. This holding mechanism, such as a strap is designed help hold the bite block in place while the procedure is being perform. Alternatively, the strap can be used to also help hold tubes or instruments being used in place to minimize harm to a patient or disruption to the procedure.
[0032] The bite block 1 may be formed from a resilient material that has strength to withstand an evoked biting response. The material should also be soft enough to prevent damage to the gums, lips, teeth, if a biting response is evoked. The bite block 1 material has enough strength to withstand and resist biting force, preventing a patient from biting down on a tube placed through a side aperture 60A or 60B or center cutout 50 in the bite block 1. The bite block 1 may be formed from a pliable material such as rubber, polyvinylidene fluoride or polyvinylidene difluoride (PVDF), or other polymers known in the art. In further embodiments the bite block may be formed from more than one type of material to allow for a more pliable outer surface with a more ridged inner configuration to withstand a biting response. The more pliable outer surface can be configured to allow for a user's teeth be held securely and communicate with the bite block. In some embodiments the bite block 1 may be placed in patients that are imaged using MRI. Bite blocks used during MRI may be formed from a non-ferrous material. The bite block 1 may be translucent, allowing a user to see through the bite block 1. The bite block 1 may also be formed from a radiolucent material to allow for imaging. In one embodiment, the bite block 1 is single use. Embodiments of the bite block 1 may be compostable. In compostable embodiments, the bite block 1 may be formed from a compostable material known in the art. In an additional embodiment the bite block 1 may be reusable. Reusable embodiments of the bite block 1 may be formed from a material suitable for reprocessing. Reusable bite blocks 1 may be formed from silicone or any other material that can withstand reprocessing or sterilization.
[0033] In an additional embodiment the bite block 1 may be formed from separable sections allowing the bite block 1 to be customizable. In some embodiments, the legs 7A and 7B are separable from the middle section 70. In other embodiments each of the legs 7A and 7B may be configured to be separated into sub pieces allowing the legs 7A and 7B to be shortened depending on the desired length. In this regard, the bite block 1 may be separable and/or configured with score lines to allow for size customization. In this regard, the bite block 1 may be customizable according to the patient's mouth size, shape, and number of teeth.
[0034] As shown in
[0035] The bite block 101 has a first end 105A and a second end 105B. The bite block 101 has a top surface 110 opposite a lower surface 120. The bite block 101 also has an interior side 130 opposite an outer side 140. The bite block 1 further includes a first leg 107A and a second leg 107B joined together by a middle section 170. The middle section 170 may include a middle cutout 150 and side apertures 160A and 160B.
[0036] As shown in
[0037] As shown in the figures, the top surface 110 may be rough to prevent the bite block 101 from slipping while in the mouth of the patient. The top surface 110 may be rough. The entire bottom surface 120 may be rough. As shown the top surface 110 of the first leg 107A and the second leg 107B may have a first ridged section 115A and a second ridged section 115B to prevent the bite block 101 from slipping while in a patient's mouth.
[0038] As shown in the figures, the middle section 170 of the bite block 101 may have a center cutout 150. The middle cutout 150 may be used to accept an endotracheal tube 222 or other instruments and/or items that will be in used during a patient's procedure. As shown in
[0039] The first and second side apertures 60A and 60B or the first and second side cutouts 160A and 160B may have a cross section that allows the cutout to accept and hold tubes with various diameters. In some cases the first and second side apertures 60A and 60B or first and second side cutouts 160A and 160B may be configured to accept tubes with a diameter of 10 mm, while in other cases the first and second side apertures 60A and 60B or the first and second side cutouts 160A and 160B are configured to accept tubes with a diameter of 4 mm, 5 mm, 6 mm, 7 mm, 8 mm, 9 mm, 11 mm, 12 mm, 13 mm, 14 mm, 15 mm, 16 mm, 17 mm, 18 mm, 19 mm, 20 mm, or greater than 20 mm.
[0040] The center aperture 50 or center cutout 150 may have a cross section that allows the center aperture 50 or center cutout 150 to accept and hold tubes with various diameters. In some cases the center cutout 150 may be configured to accept tubes with a diameter of 10 mm, while in other cases the center cutout 150 are configured to accept tubes with a diameter of 4 mm, 5 mm, 6 mm, 7 mm, 8 mm, 9 mm, 11 mm, 12 mm, 13 mm, 14 mm, 15 mm, 16 mm, 17 mm, 18 mm, 19 mm, or 20 mm.
[0041] The bite block 1, 101 may be formed from a single piece of material. In some embodiments, the bite block may be two, three, four, or more pieces joined together. By non-limiting example, the first and second legs 7A and 7B, 107A and 107B may be subpart pieces joined to the middle section 70, 170 by melting the pieces together. Each section or piece may be formed using injection molding. One of skill in the art will appreciate that the bite block may be formed using any manufacturing technique known in the art. One of skill in the art will appreciate that the bite block 1 may be formed of any biocompatible material known in the art. The bite block 1, 101 may be different sizes based on the user.
[0042] The bite block 1 may have different sizes for accommodating different mouth sizes. By way of non-limiting example, the bite block 1 may be small, medium, or large. In various embodiments, the legs 7A, 107A and 7B, 107B may have different lengths according the size of the patient's mouth. Similarly, the middle section 70, 170 may have different lengths according the size of the patient's mouth. Additionally, the thickness of the bite block 1, 101 may vary depending on the size of the patient's mouth.
[0043] The bite block 1, 101 may be used by an anesthetized patient. In some embodiments, the bite block 1, 101 may be placed in a patient's mouth after the patient is anesthetized and intubated. Next, an endotracheal tube may be prepared for deployment by removing an endotracheal tube connector. The endotracheal tube 222 may then be placed or pushed into the center cutout 50, 150. The endotracheal tube connector may then be reattached to the endotracheal tube. The endotracheal tube connector may be reattached to the endotracheal tube. The patient may then be connected to an anesthesia breathing circuit. An endotracheal tube pilot balloon may then be received by the first or second side aperture 60A or 60B. In some embodiments, an endotracheal tube pilot balloon may be threaded or pushed through or into the first or second side cutouts 160A and 160B. One of skill in the art will appreciate that the pilot balloon, the endotracheal tube 222, or any other tube used with the bite block 1, 101 may be placed in the middle cutout 50, 150 or either side aperture 60A or 60B, or either side cutout 160A or 160B. The endotracheal tube 222 may then be secured to the patient using tape, other adhesives, or any other traditional means for securing the tube to a patient. Because the bite block 1, 101 may be used with patients in a prone position, the user may place a strap around the posterior neck/head of the patient and affix the strap to the side protuberances on the bite block 1, 101. Attaching a strap to the side protuberances may aid the bite block 1, 101 in remaining in place when the patient is turned prone. One of skill in the art will appreciate that the bite block 1, 101 may remain in place without the assistance of a strap. Next, the practitioner may insert other monitoring devices, including temperature probes, through the side apertures of the bite block 1, 101. As the patient emerges from anesthesia, the user may leave the bite block in place until or after the endotracheal tube 222 is removed. The side apertures 60A or 60B or side cutouts 160A or 160B may be used for accessing the patient's mouth to with suction devices to remove oral secretions.
[0044] It is believed that the present disclosure and many of its attendant advantages will be understood by the foregoing description, and it will be apparent that various changes may be made in the form, construction, and arrangement of the components without departing from the disclosed subject matter or without sacrificing all its material advantages. The form described is merely explanatory, and it is the intention of the following claims to encompass and include such changes.
[0045] While the present disclosure has been described with reference to various embodiments, it will be understood that these embodiments are illustrative and that the scope of the disclosure is not limited to them. Those skilled in the art will appreciate that variations from the specific embodiments disclosed above are contemplated by the invention. Many variations, modifications, additions, and improvements are possible. More generally, embodiments in accordance with the present disclosure have been described in the context of implementations. Functionality may be separated or combined in blocks differently in various embodiments of the disclosure or described with different terminology. These and other variations, modifications, additions, and improvements may fall within the scope of the disclosure as defined in the claims that follow.