BITE BLOCK AND ASSEMBLIES INCLUDING SAME

TECHNICAL FIELD

The present disclosure relates to the field of bite blocks and bite block assemblies for use during endoscopic procedures.

BACKGROUND

Upper endoscopy procedures are utilized to investigate, diagnose, and/or treat medical conditions relating to the upper digestive system. Such procedures typically require a flexible endoscopic tube to be inserted through the mouth, esophagus, stomach, and duodenum. Patients are often positioned on one of their sides and sedated for a period of time depending on the type of procedure. Bite blocks are often employed to prevent sedated patients from biting and damaging the endoscopic tube during the procedure.

SUMMARY

Disclosed herein is a bite block assembly for providing gases to a subject and sampling exhaled gases from the subject during an endoscopic procedure. In some implementations, the bite block assembly comprises a bite block and a nasal cannula assembly. In some implementations, the bite block comprises a main body and a mouthpiece extending outward from the main body and configured to be positioned in a mouth of the subject when the bite block is in use. In some implementations, the mouthpiece comprises a main channel configured to receive an endoscopic tube and a sampling channel configured to receive orally exhaled gases from the subject. In some implementations, the nasal cannula assembly comprises: a nasal cannula manifold comprising a first end, a second end opposite the first end, a first interior portion, a second interior portion, a wall separating the first and second interior portions, and an opening in fluid communication with the second interior portion; a first gas delivery tube connected to the first end of the nasal cannula manifold and in fluid communication with the first interior portion of the nasal cannula manifold; a first nasal prong in fluid communication with the first interior portion of the nasal cannula manifold and configured to direct gases from the first gas delivery tube into a first nostril of the subject; a second nasal prong in fluid communication with the second interior portion of the nasal cannula manifold and configured to receive gases exhaled from a second nostril of the subject; a scoop configured to be connected to the nasal cannula manifold and direct said orally exhaled gases from the sampling channel of the bite block to the opening of the nasal cannula manifold; and a gas sampling tube. In some implementations, the scoop comprises: a body comprising a first surface and a second surface opposite the first surface, the first surface configured to face at least partially toward the sampling channel of the bite block when the bite block assembly is in use; and a rib extending outward from and along a portion of the first surface of the body, the rib defining a fluid passage configured to receive and direct said orally exhaled gases towards the opening of the nasal cannula manifold. The gas sampling tube can be connected to the second end of the nasal cannula manifold and in fluid communication with the second interior portion of the nasal cannula manifold. The gas sampling tube can be configured to direct said gases exhaled from the second nostril and said orally exhaled gases to a gas monitoring device.

In some implementations: the body of the scoop comprises a basin shape; the first surface comprises an interior surface of the basin shaped body and the second surface comprises an exterior surface of the basin shaped body; the basin shaped body further comprises an edge surface between the interior and exterior surfaces and extending along a plane; and the rib is spaced inward from said plane. In some implementations, the rib comprises an opening into the fluid passage of the rib, and wherein said opening of the rib faces away from the interior surface of the basin shaped body. In some implementations, an axis extending through a center of the opening of the rib is substantially perpendicular relative to a portion of the interior surface of the basin shaped body. In some implementations: the rib comprises a first end, a second end, and a length extending between the first and second ends; the first end of the rib terminates at a portion of the interior surface that is spaced inward from the edge surface of the basin shaped body; and an axis extending through a center of the opening of the rib is substantially perpendicular relative to the portion of the interior surface. In some implementations: the fluid passage of the rib comprises a first portion and a second portion, the first portion comprising said opening of the rib; and the first and second portions of the fluid passage of the rib are oriented transverse relative to one another. In some implementations, the first and second portions of the fluid passage of the rib are oriented substantially perpendicular relative to one another.

In some implementations, the scoop further comprises a connector extending outward from the body of the scoop and configured to connect to a portion of the nasal cannula manifold. In some implementations, said connector of the scoop is configured to secure within the opening of the nasal cannula manifold, and wherein said connector comprises a fluid passage in fluid communication with the fluid passage of the rib of the scoop. In some implementations, the rib comprises an opening into the fluid passage of the rib, and wherein the fluid passage of said connector is oriented transverse relative to the opening of the rib.

In some implementations, the bite block assembly further comprises: a second gas delivery tube configured to receive gases from a gas source; a branched connector comprising a first branch configured to be connected to the second gas delivery tube, a second branch configured to be connected to said first gas delivery tube, and a third branch configured to be connected to a third gas delivery tube; said third gas delivery tube; and a gas delivery channel in a portion of the bite block and configured to receive a portion of said third gas delivery tube; wherein the branched connector is configured to direct gases from said second gas delivery tube to the first and third gas delivery tubes when connected therewith. In some implementations, said first branch is permanently secured to said second gas delivery tube. In some implementations, said second branch is permanently secured to said first gas delivery tube. In some implementations, said third branch is configured to be removably connected to said third gas delivery tube.

In some implementations, said third gas delivery tube comprises a first end and a second end, said first end permanently secured within said gas delivery channel in the portion of the bite block. In some implementations, said second end of said third gas delivery tube is configured to be removably connected to said third branch. In some implementations, the bite block assembly further comprises a connector secured to the second end of said third gas delivery tube and having a tapered end configured to secure within the third branch. In some implementations, the bite block assembly further comprises a cap secured to the third branch, wherein the cap is configured to be transitioned from a first configuration in which the cap prevents gases from flowing out of the third branch to a second configuration in which the cap allows gases to flow out of the third branch. In some implementations, the cap comprises a base secured to the third branch, a lid, and a hinge between the base and lid and configured to allow the lid to move between an open position and a closed position. In some implementations, the cap further comprises a plug extending outward from the lid and configured to secure within an opening in the third branch when the lid in in the closed position.

In some implementations, said gas delivery channel is in fluid communication with the main channel of the bite block. In some implementations, an axis extending through a center of said gas delivery channel is oriented transverse relative to an axis extending through a center of said main channel. In some implementations, said gas delivery channel opens into the main channel. In some implementations, said gas delivery channel is formed from a recess on a portion of a surface of the main body and a hole extending through the main body and through a portion of the mouthpiece.

In some implementations: said main body of said bite block comprises an opening in fluid communication with the sampling channel of the mouthpiece; said bite block further comprises a pocket wall extending outward from the main body and around said opening in the main body; and said scoop is configured to fit at least partially within an interior space defined by said pocket wall and direct said orally exhaled gases from the sampling channel to the opening of the nasal cannula manifold.

In some implementations, the nasal cannula manifold comprises a first arm, a second arm, and a body positioned between the first and second arms, and wherein the first and second nasal prongs extend from the body. In some implementations, each of the first and second arms comprises a bent portion. In some implementations, the first and second arms are removably connectable to the body. In some implementations, the first gas delivery tube is connected to the first arm and wherein the gas sampling tube is connected to the second arm.

In some implementations, the opening of the nasal cannula manifold is in said body. In some implementations, the nasal cannula manifold further comprises a connector extending outward from the body and configured to receive and secure a connector of the scoop. In some implementations, the connector of the nasal cannula manifold and the connector of the scoop connect in a friction fit arrangement. In some implementations, an interior of the connector of the nasal cannula manifold is in fluid communication with the opening of the nasal cannula manifold.

In some implementations, the nasal cannula manifold further comprises a connector configured to receive and secure a connector of the scoop. In some implementations, the connector of the nasal cannula manifold and the connector of the scoop connect in a friction fit arrangement. In some implementations, an interior of the connector of the nasal cannula manifold is in fluid communication with the opening of the nasal cannula manifold. In some implementations, the bite block assembly further comprises a flange extending outward from a portion of the nasal cannula manifold and configured to assist in positioning the scoop relative to the nasal cannula manifold when the scoop is connected to the nasal cannula manifold. In some implementations, the bite block assembly further comprises a wall extending through a portion of the mouthpiece and configured to divide the main channel from the sampling channel. In some implementations, the mouthpiece comprises a first end connected to the main body, a second end opposite the first end, and a length extending between the first and second ends, wherein a length of the sampling channel is less than the length of the mouthpiece.

In some implementations, the main body of the bite block comprises a first wing, a second wing, and an intermediate portion between the first and second wings, and wherein the first and second wings are configured to extend laterally away from the subject's mouth and contact the subject's face when the mouthpiece is positioned in the subject's mouth. In some implementations, the bite block assembly further comprises a strap configured to secure the bite block to the subject's head, wherein each of the first and second wings comprises a hook configured to attach to a portion of the strap.

Disclosed herein is a bite block assembly for providing gases to a subject and sampling exhaled gases from the subject during an endoscopic procedure. In some implementations, the bite block assembly comprises a bite block and a nasal cannula assembly. In some implementations, the bite block comprises a main body and a mouthpiece extending outward from the main body and configured to be positioned in a mouth of the subject when the bite block is in use. In some implementations, the mouthpiece comprises: a main channel configured to receive an endoscopic tube; and a sampling channel configured to receive orally exhaled gases from the subject. In some implementations, the nasal cannula assembly comprises: a nasal cannula manifold comprising a manifold body, a first nasal prong extending outward from the manifold body, and a second nasal prong extending outward from the manifold body and spaced from the first nasal prong, wherein a first portion of the manifold body is configured to direct gases received from a gas delivery tube to the first nasal prong, and wherein a second portion of the manifold body is configured to direct exhaled gases received by the second nasal prong to a gas sampling tube; and a scoop configured to be connected to the nasal cannula manifold and direct said orally exhaled gases from the sampling channel of the bite block to the second portion of the manifold body. In some implementations, the scoop comprises: a body comprising a first surface and a second surface opposite the first surface, the first surface configured to face at least partially toward the sampling channel of the bite block when the bite block assembly is in use; and a rib extending outward from and along a portion of the first surface of the body, the rib defining a fluid passage configured to receive and direct said orally exhaled gases towards the second portion of the manifold body.

In some implementations, the first portion of the manifold body is not in fluid communication with the second portion of the manifold body. In some implementations, the manifold body further comprises an inner wall that partitions an interior of the manifold body into the first and second portions. In some implementations, the nasal cannula assembly further comprises said gas delivery tube, and wherein said gas delivery tube is connected to a first end of the manifold body and is configured to receive gases from a gas source. In some implementations, the nasal cannula assembly further comprises said gas sampling tube, and wherein said gas sampling tube is connected to a second end of the manifold body and is configured to direct said gases exhaled from the subject to a gas monitoring device. In some implementations, the manifold body further comprises an opening in fluid communication with the second portion of the manifold body, and wherein the fluid passage of the rib of the scoop is in fluid communication with the opening and second portion of the manifold body when the scoop is connected to the nasal cannula manifold.

Disclosed herein is a bite block comprising: a main body comprising a first surface and a second surface opposite the first surface; and a mouthpiece extending outward from the second surface of the main body and configured to be positioned in a mouth of the subject when the bite block is in use. In some implementations, the mouthpiece comprises: a main channel configured to receive an endoscopic tube; and a sampling channel configured to receive orally exhaled gases from the subject. In some implementations, the bite block further comprises a gas delivery channel configured to direct gases into the subject's mouth when the bite block is in use, the gas delivery channel extending through a portion of the main body and through a portion of the main channel such that the gas delivery channel is in fluid communication with the main channel. In some implementations, the bite block further comprises a recess extending along a portion of the first surface of the main body proximate the gas delivery channel, wherein the recess is configured to receive a portion of a gas delivery tube.

In some implementations, an axis extending through a center of the gas delivery channel is transverse relative to an axis extending through a center of the main channel. In some implementations, the bite block further comprises a tube clip extending outward from a portion of the main body, the tube clip configured to secure a portion of the gas delivery tube. In some implementations: the main body further comprises a first wing, a second wing, and an intermediate portion between the first and second wings; the first and second wings are configured to extend laterally away from the subject's mouth and contact the subject's face when the mouthpiece is positioned in the subject's mouth; the tube clip extending outward from the first surface and the first wing of the main body. In some implementations, the tube clip comprises a first arm and a second arm spaced from the first arm, and wherein free ends of the first and second arms are spaced away from one another by a gap, thereby allowing the first and second arms to be resiliently flexed to secure the portion of the gas delivery tube to the tube clip.

Disclosed herein is a bite block comprising a main body, a mouthpiece, and a gas delivery channel. The main body can comprise a first surface and a second surface opposite the first surface, a first wing, a second wing, and an intermediate portion between the first and second wings, the first and second wings extending laterally away from the intermediate portion. The mouthpiece can extend outward from the second surface of the main body and be positioned in a mouth of a subject when the bite block is in use. In some implementations, the first and second wings of the main body are configured to be positioned on opposite sides of the subject's mouth and adjacent the subject's face when the mouthpiece is positioned in the subject's mouth. In some implementations, the mouthpiece comprises: a main channel configured to receive an endoscopic tube; and a sampling channel configured to receive orally exhaled gases from the subject. The bite block can further comprise: a gas delivery channel configured to direct gases into the subject's mouth when the bite block is in use, the gas delivery channel extending through the intermediate portion of the main body and through a portion of the main channel of the mouthpiece such that the gas delivery channel is in fluid communication with the main channel. The bite block can further comprise: a gas delivery tube configured to deliver gases to the gas delivery channel, the gas delivery tube comprising a first end and a second end opposite the first end, wherein the second end is permanently secured within the gas delivery channel. The bite block can further comprise: a tube clip located on a portion of the first wing of the main body, the tube clip comprising a first arm and a second arm, each of the first and second arms extending outward from the first wing and having free ends that are separated from one another by a gap, wherein the first and second arms are configured to secure a first portion of the gas delivery tube. The bite block can further comprise: a recess extending along a portion of the first surface of the main body proximate the gas delivery channel, wherein the recess is configured to receive a second portion of the gas delivery tube when the first portion of the gas delivery tube is secured between the first and second arms of the tube clip.

In some implementations, an axis extending through a center of the gas delivery channel is transverse relative to an axis extending through a center of the main channel. In some implementations, a first end of the recess is located at the gas delivery channel and a second end of the recess is spaced away from the gas delivery channel. In some implementations, the recess extends from the first end to the second end, and wherein the second end of the recess is located at a junction where the first wing and the intermediate portion of the main body meet. In some implementations, the recess extends from the gas delivery channel along the intermediate portion and toward the first wing. In some implementations, the recess extends from the gas delivery channel along the intermediate portion and toward the tube clip. In some implementations, the recess comprises a substantially semi-circular cross-section. In some implementations, the recess is configured to surround less then an entire cross-section of the first portion of the gas delivery tube. In some implementations, the recess is configured to surround less then about ¾ of a cross-section of the first portion of the gas delivery tube. In some implementations, a first portion of the gas delivery channel comprises a first cross-section and a second portion of the gas delivery channel comprises a second cross-section that is different than the first cross-section. In some implementations, a ledge is defined at a juncture of the first and second cross-sections of the gas delivery channel, and wherein the second end of the gas delivery tube abuts the ledge.

Disclosed herein is a bite block comprising a main body and a mouthpiece. The main body can comprise a first surface and a second surface opposite the first surface. The mouthpiece can extend outward from the second surface of the main body and be configured to be positioned in a mouth of a subject when the bite block is in use. The mouthpiece can comprise: a main channel configured to receive an endoscopic tube; and a sampling channel configured to receive orally exhaled gases from the subject. The bite block can further comprise a gas delivery channel configured to direct gases into the subject's mouth when the bite block is in use, the gas delivery channel extending through a portion of the main channel of the mouthpiece such that the gas delivery channel is in fluid communication with the main channel. The bite block can further comprise a recess extending along a portion of the first surface of the main body proximate the gas delivery channel, wherein the recess is configured to receive a portion of a gas delivery tube.

In some implementations, an axis extending through a center of the gas delivery channel is transverse relative to an axis extending through a center of the main channel. In some implementations, a first end of the recess is located at the gas delivery channel and a second end of the recess is spaced away from the gas delivery channel. In some implementations, the main body comprises a first wing, a second wing, and an intermediate portion between the first and second wings, and wherein the second end of the recess is located at a junction where the first wing and the intermediate portion of the main body meet. In some implementations, the recess comprises a substantially semi-circular cross-section. In some implementations, the recess is configured to surround less then an entire cross-section of the portion of the gas delivery tube. In some implementations, the bite block further comprises a tube clip located on a portion of the main body, the tube clip comprising a first arm and a second arm, each of the first and second arms extending outward from the portion of the main body and having free ends that are separated from one another by a gap, wherein the first and second arms are configured to secure the gas delivery tube. In some implementations, a first portion of the gas delivery channel comprises a first cross-section and a second portion of the gas delivery channel comprises a second cross-section that is different than the first cross-section. In some implementations, the bite block further comprises said gas delivery tube, said gas delivery tube comprising a first end and a second end, wherein a ledge is defined at a juncture of the first and second cross-sections of the gas delivery channel, and wherein the second end of the gas delivery tube abuts the ledge.

For purposes of summarizing the disclosure, certain aspects, advantages and novel features of several devices, systems, and methods have been described herein. It is to be understood that not necessarily all examples of the present disclosure are disclosed herein. Thus, the devices, systems, and methods disclosed herein can be embodied or carried out in a manner that achieves or optimizes one advantage or group of advantages as taught herein without necessarily achieving other advantages as can be taught or suggested herein.

BRIEF DESCRIPTION OF THE DRAWINGS

Certain features of this disclosure are described below with reference to the drawings. The illustrated embodiments are intended to illustrate, but not to limit the embodiments. Various features of the different disclosed embodiments can be combined to form further embodiments, which are part of this disclosure.

FIG. 1A illustrates a front view of a bite block assembly in accordance with aspects of this disclosure.

FIGS. 1B-1D illustrate enlarged views of portions of the bite block assembly of FIG. 1A in accordance with aspects of this disclosure.

FIG. 1E illustrates a back view of the portion of the bite block assembly shown FIG. 1D in accordance with aspects of this disclosure.

FIG. 1F illustrates a cross-section taken through a portion of the bite block assembly shown FIGS. 1D-1E in accordance with aspects of this disclosure.

FIG. 2 illustrates portions of the bite block assembly of FIG. 1A separated from one another in accordance with aspects of this disclosure.

FIG. 3 illustrates a bite block and gas delivery tube of the bite block assembly of FIG. 1A in accordance with aspects of this disclosure.

FIG. 4A illustrates a back view of the bite block of FIG. 3 in accordance with aspects of this disclosure.

FIGS. 4B-4C illustrate side views of the bite block of FIG. 3 in accordance with aspects of this disclosure.

FIGS. 4D-4E illustrate top and bottom views of the bite block of FIG. 3 in accordance with aspects of this disclosure.

FIGS. 4F-4J illustrate perspective views of the bite block of FIG. 3 in accordance with aspects of this disclosure.

FIG. 5 illustrates a partially exploded view of a nasal cannula assembly of the bite block assembly of FIG. 1A in accordance with aspects of this disclosure.

FIGS. 6A-6B illustrate enlarged views of a branched connector of the nasal cannula assembly of FIG. 5 in accordance with aspects of this disclosure.

FIGS. 7A-7D illustrate enlarged views of a scoop of the nasal cannula assembly of FIG. 5 in accordance with aspects of this disclosure.

FIGS. 8A-8C illustrate enlarged views of a nasal cannula manifold of the nasal cannula assembly of FIG. 5 in accordance with aspects of this disclosure.

FIGS. 8D-8E illustrate exploded views of the nasal cannula manifold of FIGS. 8A-8C in accordance with aspects of this disclosure.

FIG. 8F illustrates a cross-section taken through a portion of the nasal cannula manifold shown in FIG. 8C.

FIG. 9A illustrates a front view of a bite block assembly in accordance with aspects of this disclosure.

FIGS. 9B-9D illustrate enlarged views of a branched connector of the bite block assembly of FIG. 9A in accordance with aspects of this disclosure.

DETAILED DESCRIPTION

Various embodiments will be described below in conjunction with the drawings for purposes of illustration. It should be appreciated that many other implementations of the disclosed concepts are possible, and various advantages can be achieved with the disclosed implementations.

Disclosed herein are bite block assemblies, bite blocks, nasal cannula assemblies, and components thereof which can be used during an endoscopic procedure to: deliver gases (for example, oxygen) to a subject's oral and/or nasal passages; and/or collect exhaled gases (which can include, for example, CO₂) from the subject's oral and/or nasal passages for analysis and/or monitoring, for example, for capnography and/or anesthetic gas measurements.

FIG. 1A illustrates a bite block assembly 1. FIG. 1D illustrates an enlarged view of a nasal cannula assembly 15 and a bite block 100, and FIGS. 1B-1C illustrate enlarged views of portions of gas delivery tube 2, 6, gas sampling tubes 4, 8, and couplers and connectors connected to portions thereof. Bite block 100 can be utilized to facilitate insertion of an endoscopic tube into a subject's mouth and inhibit (for example, prevent) the subject from biting down on the endoscopic tube. As discussed further below, bite block 100 can include a main body and a mouthpiece extending outward from the main body, and such mouthpiece can include a main channel that allows such endoscopic tube to be inserted into the subject's mouth during a procedure and, at the same time, prevent the subject's mouth from closing on the endoscopic tube, thereby avoiding damage to the tube and/or interference with the procedure. Such main body of the bite block can rest outside the subject's mouth when the mouthpiece is positioned in the mouth, and, in some implementations, can be secured to the subject's head (for example, with a strap as discussed below).

As discussed further below, a nasal cannula assembly 15 can be utilized alongside the bite block 100 in order to: deliver gases to one or more of the subject's nostrils; and/or collect exhaled gases from one or more of the nostrils for sampling. With reference to at least FIGS. 1D-1E, the nasal cannula assembly 15 can include a gas delivery tube 18 connected to a first portion (for example, a first end) of a nasal cannula manifold 30, prongs 32a, 32b for delivering gases (for example, oxygen) and/or collecting gases exhaled from the subject's nostrils, and a gas sampling tube 8 connected to a second portion (for example, a second end) of the nasal cannula manifold 30. Bite block 100 can be utilized for oral delivery of gases (for example, oxygen) to the subject's mouth and/or for collecting orally exhaled gases from the subject's mouth. The nasal cannula assembly 15 and the bite block 100 can interact with and/or engage one another in order to accomplish oral and/or nasal gas delivery and/or exhaled gas sampling. For example, in some implementations, bite block assembly 1 includes a branched connector 16 that allows gases from a gas source to be split between tube 18 (for delivery to the nasal cannula manifold 30) and a gas delivery tube 22 that can be connected to a portion of the bite block 100 for delivery of such gases into the subject's mouth. As another example, in some implementations, a scoop 50 (which can be included in nasal cannula assembly 15) connected to the nasal cannula manifold 30 can be utilized to guide orally exhaled gases from a sampling channel of bite block 100 (such as sampling channel 114 discussed further below) to the nasal cannula manifold 30 for sampling. As discussed further below, the scoop 50 can be sized and/or shaped to fit within a region formed by a pocket wall extending outward from and along a portion of the main body of the bite block 100 around the sampling channel of bite block 100. Such pocket wall can be wall 112 described further below.

Advantageously, the nasal cannula assembly 15 and the bite block 100 can be removable from one another, thereby allowing the nasal cannula assembly 15 to continue to be utilized (for gas delivery and/or exhaled gas sampling) before, during, and after the bite block 100 is positioned within the subject's mouth. For example, in some implementations, the scoop 50 does not secure (for example, connect) to the bite block 100, but rather, rests and/or is otherwise positioned in a space defined by a pocket wall (for example, wall 112) of bite block 100. In some implementations, a connector 20 (which can be permanently or removably connected to tube 22) can removably secure within a branch 16c of branched connector 16, as shown in FIGS. 1D-1E and FIG. 2. As also discussed further below, when such branch 16c (see FIGS. 6A-6B) is closed and/or not connected to connector 20, such branch 16c can be manually closed with a cap 24 so that delivery gases are only directed toward branch 16b, tube 18, and the nasal cannula manifold 30. With reference to FIG. 3, in some implementations, connector 20 has a body 20a and a tapered end 20b connected to body 20a, and tapered end 20b is sized and/or shaped to fit within (for example, via a friction fit arrangement) branch 16c of branched connector 16 (see FIG. 6A).

With reference to FIG. 2, nasal cannula assembly 15 can include a gas delivery tube 18, a nasal cannula manifold 30, a gas sampling tube 8, and/or a branched connector 16 as discussed above. With reference to FIG. 1B, in some implementations, nasal cannula assembly 15 additionally includes a coupler 10 that can retain tubes 6, 8. Coupler 10 can have a rounded (for example, cylindrical) shape and can be configured to receive tubes 6, 8. In some implementations, nasal cannula assembly 15 includes a coupler 12 that joins gas delivery tube 6 with another gas delivery tube 2 and/or that joins gas sampling tube 8 with gas sampling tube 4. In some implementations, gas delivery tubes 6 and 2 are different, for example, have different cross-sections. In some implementations, gas sampling tubes 8 and 4 are different, for example, have different cross-sections. With reference to FIG. 1C, a connector 2a can be located at an end of tube 2. Connector 2a can be connected to a portion of a gas source (for example, an oxygen gas source). As also shown, a connector 14 can be positioned on an end of tube 4 for connecting to a monitoring device. In some implementations, connector 14 includes moisture wicking structure configured to wick moisture away from the subject's exhaled gases and/or includes a hydrophobic bacteria filter.

FIG. 3 illustrates a front view of bite block 100 and gas delivery tube 22 disconnected from one another. As discussed further below, in some implementations, gas delivery tube 22 is permanently secured to bite block 100 (for example, within recess 111 and/or gas delivery channel 110). With reference to FIGS. 3-4J, bite block 100 can include a main body 102 and a mouthpiece 104. Mouthpiece 104 can extend outward from the main body 102, for example, from a first surface (which may also be referred to herein as a “rear surface”) of the main body 102 that faces toward the subject when bite block 100 is in use. Main body 102 can include a second surface (which may also be referred to herein as a “front surface”) opposite such first surface which faces away from the subject when the mouthpiece 104 is positioned in the subject's mouth. Portions of the main body 102 can rest outside and/or contact portions of the subject's face around the mouth (for example, the subject's lips) and prevent mouthpiece 104 from moving further into the subject's mouth. For example, portions of main body 102 around (for example, above and below) the opening 102b (see FIG. 3) and/or opening 116 (see FIGS. 4F-4G) can rest outside and/or contact the lips of the subject when mouthpiece 104 is positioned within the subject's mouth. Such portions of main body 102 that rest outside and/or contact the subject's lips when mouthpiece 104 is positioned in the subject's mouth can be an intermediate portion 102a discussed below.

FIGS. 3-4J illustrate various views of bite block 100. As mentioned above, bite block 100 can include main body 102 and mouthpiece 104 extending outward form main body 102. Main body 102 can include wings 106, 108 and an intermediate portion 102a positioned between wings 106, 108. Wings 106, 108 can extend outward from intermediate portion 102a in opposite directions and can be positioned on opposite sides of the subject's mouth when bite block 100 is in use. In some implementations, wings 106, 108 cooperate with a strap 3 (see FIG. 1A) to secure the bite block 100 to the subject's head. For example, strap 3 can include a plurality of holes (see FIG. 1A) configured to receive strap hooks 106a, 108a extending from wings 106, 108. Strap hooks 106a, 108a can extend at least partially inward from ends of wings 106, 108 (see FIGS. 4D-4E). Wings 106, 108 can include openings 106c, 108c that can receive portions of strap 3 to facilitates securement with strap hooks 106a, 108a. In some implementations, bite block 100 includes flexible hinges 106d, 108d that can improve flexibility of wings 106, 108, for example, relative to intermediate portion 102a of main body 102. Such hinges 106d, 108d can be defined by reduced cross-section portions on the wings 106, 108, for example, at or near a region where wings 106, 108 connect to intermediate portion 102a. In such implementations, such hinges 106d, 108d may be referred to as living hinges.

In some implementations, bite block 100 includes one or more tube clips configured to secure a portion of gas delivery tube 22. For example, with reference to at least FIGS. 3, 4B, and 4D-4H, bite block 100 can include a tube clip 106e. Tube clip 106e can include two arms that extend from a portion of main body 102 (for example, from a surface of wing 106). Such two arms can be separated from one another, and free ends of such arms of tube clip 106e can be spaced from one another by a gap. Such configuration can allow the two arms to be moved (for example, flexed) away from one another to facilitate positioning of a portion of tube 22 therebetween. Such two arms can be resilient. Accordingly, in some implementations, tube clip 106e does not surround an entire cross-section of the tube 22 when tube 22 is secured thereto. With reference to FIG. 4A, in some implementations, an opening 106f in wing 106 is positioned adjacent the two arms of tube clip 106e. Opening 106f can allow the portion of tube 22 secured by tube clip 106e to be more easily moved (for example, pushed) out of securement with tube clip 106e. In some implementations, bite block 100 only includes one tube clip configured to secure a portion of gas delivery tube 22 (which can be, for example, tube clip 106e).

With reference to FIGS. 3, 4A, and 4F-4J, mouthpiece 104 can include a main channel 104a. Main channel 104a can be defined at least partially by an opening 102b in main body 102 (see FIG. 3). For example, opening 102b can form a first end of main channel 104a. Mouthpiece 104 can have a first end connected to main body 102 and a second, opposite end that terminates a distance away from main body 102 (see FIGS. 4D-4E). Main channel 104a can be utilized to allow a tube (for example, an endoscopic tube) to be inserted through bite block 100 and into a subject's mouth (and into other regions of the subject's body) during a procedure. With reference to at least FIGS. 4B-4E, in some implementations, mouthpiece 104 includes protrusions 104b, 104c that can interact with teeth and/or other portions of the subject's mouth to facilitate proper positioning and/or orientation of bite block 100 when in use. Protrusions 104b, 104c can extend outward from a portion of (for example, an exterior surface of) mouthpiece 104 and can extend along a portion of a width of mouthpiece 104 (see FIGS. 4D-4E). In some implementations, protrusions 104b, 104c are positioned at the second (“free”) end of mouthpiece 104.

Bite block 100 can include a gas delivery channel to allow gases (for example, oxygen) to be delivered to the subject's mouth when bite block 100 is in use, and such oral gas delivery can be in addition to or as an alternative to gas delivery via the nasal cannula assembly 15 (via the subject's nostrils) discussed elsewhere herein. This is advantageous since many subjects breath via oral inhalation either primarily or in a supplementary manner along with nasal inhalation. With reference to at least FIGS. 3-4B, 4D-4J, bite block 100 can include a gas delivery channel 110. Gas delivery channel 110 can extend through a portion of main body 102 and/or a portion of mouthpiece 104. For example, with reference to FIG. 3, gas delivery channel 110 can extend through a portion of main body 102 proximate to opening 102b. FIGS. 4A, 4D-4E, and 4I-4J illustrate an outer portion (which also may be referred to herein as “outer structure”) that at least partially defines gas delivery channel 110. As shown in at least FIGS. 4A, 4D-4E, and 4I, gas delivery channel 110 can be at least partially defined along an outer portion of the mouthpiece 104, for example, at a region where mouthpiece joins main body 102. Gas delivery channel 110 can extend transverse relative to opening 102b of main body 102 and/or mouthpiece 104. For example, an axis extending through a center of gas delivery channel 110 (see FIG. 4H) can be transverse to an axis extending through a center of mouthpiece 104 and/or an axis extending through opening 102b of main body 102. As shown in FIG. 4J, gas delivery channel 110 can terminate inside the mouthpiece 104, for example, inside main channel 104a. The opening of the gas delivery channel 110 into main channel 104 can be angled, as shown in FIG. 4J. Accordingly, gas delivery channel 110 can be in fluid communication with main channel 104a and can deliver gases (from tube 22) directly into main channel 104a for delivery into the subject's oral passage.

As shown in at least FIGS. 3, 4B, and 4F-4H, main body 102 can include a recess 111. Recess 111 can be recessed from a surface (for example, a “front surface”) of main body 102 opposite a surface of main body 102 from which mouthpiece 104 extends. Recess 111 can extend to gas delivery channel 110 as shown. Recess 111 can advantageously be sized and/or shaped to receive a portion of tube 22, for example, when tube 22 is connected to bite block 100 (for example, via clip 106e) and/or when an end of tube 22 is positioned within at least a portion of gas delivery channel 110. Recess 111 can therefore advantageously allow tube 22 to more easily bend, flex, and/or be positioned in gas delivery channel 110, which can minimize or prevent “kinking” of tube 22 that can interfere with oral gas delivery to the subject. Recess 111 can comprise a smooth and/or rounded surface. Recess 111 can be configured to surround less than an entire cross-section of a portion of tube 22 when secured therewith. For example, recess 111 can be configured to surround less than about ¾ of a cross-section of tube 22 when tube 22 is positioned in recess 111. In some implementations, recess 111 (or at least a portion thereof) has a substantially semi-circular cross-section. In some implementations, recess 111 has a first end at gas delivery channel 110 and extends outward from such first end, for example, toward wing 106 and/or tube clip 106e. In some implementations, recess 111 is integrally formed with gas delivery channel 110.

Gas delivery channel 110 is defined at least partially by a cross-section that varies, for example, along a length of gas delivery channel 110. For example, gas delivery channel 110 can have a first cross-section for a portion of a length of the channel 110 and a second cross-section for another portion of the length of the channel 110. Such configuration can define a ledge 110a (see FIG. 4H). Such ledge 110a can aid the positioning, placement, and/or securement of an end of tube 22 in channel 110. In some implementations, gas delivery channel 110 has a first circular cross-section for a portion of the length of channel 110 and a second circular cross-section for another portion of the length of channel 110, thereby defining a circular ledge 110a. In some implementations, an annular ring structure is positioned within gas delivery channel 110, and one end of such annular ring structure can define the ledge 110a.

With reference to at least FIGS. 4A and 4I-4J, mouthpiece 104 can include a sampling channel 114 for collecting orally exhaled gases from a subject's mouth when bite block 100 is in use. Bite block 100 (for example, mouthpiece 104) can include a wall 113 (which may be referred to as an “inner wall”) that can separate sampling channel 114 from main channel 104a. FIG. 1F illustrates a cross-section taken through bite block 100 as well as nasal cannula assembly 15. In some implementations, such as that shown in FIG. 1F, inner wall 113 does not extend beyond an outer end of mouthpiece 104, and an end of inner wall 113 is spaced inward from the outer end of mouthpiece 104 by a distance d1. With reference to FIGS. 1F and 4F-4G, main body 102 can include an opening 116 that is in fluid communication with sampling channel 114. Opening 116 can be positioned adjacent (for example, above) opening 102b of main body 102 (see FIGS. 4F-4G).

With reference to at least FIGS. 3 and 4B-4H, bite block 100 can include a wall 112 (which may also be referred to as a “pocket wall”) extending outward from a portion of main body 102 and around opening 116 (for example, from a surface of main body 102 that faces away from the subject when bite block 100 is in use). Wall 112 can extend outward from main body 102 and adjacent to opening 102b (see FIG. 3). Wall 112 can extend around an entire width of opening 116, where such “width” of opening 116 extends in right and left directions in the view of FIG. 3. Wall 112 can at least partially define (for example, along with a portion of main body 102) a space that is sized and/or shaped to receive a portion of scoop 50 of nasal cannula assembly 15. For example, with reference to at least FIGS. 1D-1F, a portion (for example, an end) of scoop 50 can be received within a space defined by wall 112 and main body 102 around opening 116. Advantageously, orally exhaled gases can be directed by sampling channel 114 through opening 116 and towards scoop 50 when scoop 50 is positioned between wall 112 and opening 116. The collection of such exhaled gases by scoop 50 and nasal cannula assembly 15 is described further below.

FIGS. 1D-1F illustrate nasal cannula assembly 15 engaged with bite block 100 and FIG. 2 illustrates nasal cannula assembly 15 separated from bite block 100 (and separated from tube 22 and connector 20). FIG. 5 illustrates a partially exploded view of nasal cannula assembly 15. Although FIG. 5 does not illustrate tubes 2, 4, couplers 10, 12, and connectors 2a, 14, any or all of such components (which are described above) can form part of nasal cannula assembly 15, and/or nasal cannula assembly 15 can include additional or alternative components. As shown in FIG. 5, nasal cannula assembly 15 can include gas delivery tubes 6, 18, a branched connector 16, a closable cap 24 connected to the branched connector 16, a nasal cannula manifold 30 (which can include nasal prongs 32a, 32b), a scoop 50, and a gas sampling tube 8.

FIG. 6A illustrates an enlarged view of branched connector 16 and cap 24, and also illustrates portions of tubes 6, 18. Branched connector 16 can include a first branch 16a, a second branch 16b, and a third branch 16c. Branch 16a can be permanently or removably connected to tube 6. Branch 16b can be permanently or removably connected to tube 18. In some embodiments, branched connector 16 includes a flange 16d (for example, extending outward and/or along branch 16b) that can aid a user in handling branched connector 16. Branch 16c can be configured to removably connect to gas delivery tube 22, for example, via connector 20 secured to an end of tube 22. With reference to FIG. 3, branch 16c can be configured to receive a tapered end 20b of connector 20 (see FIGS. 1D-1E and 3). The securement between tapered end 20b and branch 16c can be a friction fit engagement. Alternatively, in some implementations, connector 20 is configured to secure to branch 16c via a snap fit engagement. Connection between connector 20 and branch 16c can facilitate fluid communication between tube 22 and tube 6, thereby allowing gases (for example, oxygen) to be delivered by tube 6 and branch 16c to tube 22 (and to gas delivery channel 110 in bite block 100). Branch 16b can facilitate fluid communication between tube 18 and tube 6. Branched connector 16 can include an interior defined by interiors of branches 16a, 16b, 16c, all of which can be in fluid communication with each other and with tubes 6, 18, and/or 22 when connected therewith.

With continued reference to FIGS. 6A-6B, cap 24 can be secured to a portion of branched connector 16 to enable a fluid flow path through branch 16c to be closed, for example, when connector 20 and tube 22 are not connected to branch 16c. Cap 24 can include a base 24a, a lid 24c, and a hinge 24b. Base 24a can be secured to (for example, around all or a portion of a perimeter of) branch 16c. Hinge 24b can be positioned between base 24a and lid 24c and can connect base 24a and lid 24c. Hinge 24b can allow lid 24c to move (for example, rotate) relative to base 24a. Hinge 24b can be a living hinge. In some implementations, cap 24 (for example, base 24a) is permanently secured to branched connector 16 (for example, to branch 16c). FIG. 6A illustrates cap 24 in an open position where branch 16c is in fluid communication with the ambient environment when not connected with tube 22 (via connector 20). In such open position, connector 20 (for example, tapered end 20b) can be inserted within branch 16c. FIG. 6B illustrates cap 24 in a closed position, where branch 16c is not in fluid communication with the ambient environment. With reference to FIG. 6A, in some implementations, cap 24 includes a plug 24e sized and/or shaped to fit and/or secure within branch 16c (for example, an opening into an interior defined within branch 16c). Such connection of plug 24e within branch 16c can be a friction fit arrangement, for example. In some implementations, cap 24 includes a handle 24d (which may be referred to as a “handle portion”) that can allow a user to grip and/or move (for example, rotate) lid 24c and move cap 24 between the closed and open positions.

FIGS. 7A-7D illustrate various views of scoop 50. Scoop 50 can include a body 52 having a first surface 52a and a second surface 52b opposite the first surface 52a. The first surface 52a (which may be referred to as an “outer” or “exterior” surface) can face at least partially away from the subject when nasal cannula assembly 15 is in use and the second surface 52b (which may be referred to as an “inner” or “interior” surface) can face at least partially toward the subject when nasal cannula assembly 15 is in use. When nasal cannula assembly 15 is used with bite block 100, at least a portion of inner surface 52b can face in a direction toward opening 116 and sampling channel 114 of bite block 100 (see, for example, FIG. 1F). In some implementations, such as that shown in the figures, body 52 of scoop 50 has a basin shape. For example, exterior surface 52a can have a convex shape, interior surface 52b can have a concave shape, and body 52 can have an edge surface 52c extending along a juncture of surfaces 52a, 52b and/or between surfaces 52a, 52b. As shown, portions of the interior surface 52b can be positioned inward from such edge surface 52c. Such configurations can allow scoop 50 to better receive and direct exhaled gases from sampling channel 114 and opening 116 of bite block 100.

With reference to FIGS. 7B-7C, scoop 50 can include a rib 54 extending outward from and along a portion of surface 52b. Rib 54 can extend along a middle of body 52 and/or surface 52b. Rib 54 can extend along an axis of symmetry of body 52 and/or scoop 50 (see FIG. 7C). With reference to FIG. 1F, rib 54 can include a first end having an opening into a first fluid passage 54a. Rib 54 can include a second fluid passage 54b in fluid communication with fluid passage 54a. Fluid passages 54a, 54b can be oriented transverse (for example, perpendicular) to one another. Fluid passages 54a, 54b can receive orally exhaled gases from opening 116 and sampling channel 114 of bite block 100, which can be guided (at least partially) by body 52 of scoop 50.

Scoop 50 can be configured to connect to nasal cannula manifold 30. In some implementations, scoop 50 includes a connector 56 configured to connect to a portion of nasal cannula manifold 30 (for example, to connector 32e of nasal cannula manifold 30 shown in at least FIG. 8A). Connector 56 can include an opening 56a and can include a fluid passage in fluid communication with fluid passages 54b, 54a of rib 54 (see FIG. 1F). In some implementations, scoop 50 includes a notch 53 in body 52 that includes a surface from which connector 56 extends. In some implementations, such notch 53 is sized and/or shaped to accommodate a portion of connector 32e of nasal cannula manifold 30 shown in at least FIG. 8A.

FIGS. 8A-8C illustrate enlarged views of nasal cannula manifold 30. Nasal cannula manifold 30 can include a body 32 (which may be referred to as a “manifold body”), nasal prongs 32a, 32b spaced from one another and extending outward from body 32, and arms 34, 36. Arms 34, 36 can include a bend, which may also be referred to as a “bent portion” (see FIG. 8C). Such bend can form an angle between about 0 degrees and about 90 degrees, for example, about 45 degrees. Arms 34, 36 can be permanently or removably secured to body 32. In some implementations, arms 34, 36 are integral with body 32. FIGS. 8A-8C illustrate arms 34, 36 connected to body 32, whereas FIGS. 8D-8E illustrate arms 34, 36 separated from body 32. With reference to FIGS. 8D-8E, body 32 can include slots 32d (for example, near or at ends of body 32) that are configured to receive and/or secure to protrusions 34c, 36c on ends of arms 34, 36. In some implementations, arms 34, 36 include a first portion 34a, 36a and a second portion 34b, 36b, and the first portions 34a, 36a have a different (for example, smaller) cross-section than the second portion 34b, 36b. Such configuration can allow portions 34a, 36a to be received and/or secured within ends of body 32. Interaction between slots 32d and protrusions 34c, 36c can act to position and/or secure arms 34, 36 with respect to body 32.

As shown in FIGS. 8A-8E, nasal cannula manifold 30 can include a connector 32e extending outward from body 32 and configured to connect to connector 56 of scoop 50. Connector 32e can include an opening 32f that allows connector 56 of scoop 50 to be received and/or secured within connector 32e. Connector 32e can thereby facilitate fluid communication between fluid passages 54a, 54b of rib 54 of scoop 50 and an interior portion of the nasal cannula manifold 30.

In some implementations, nasal cannula manifold 30 includes a flange 32g extending outward from body 32 and adjacent to connector 32e. Flange 32g can act to position and/or at least partially secure scoop 50 relative to nasal cannula manifold 30, for example, as shown in FIGS. 1A-2. Flange 32g can extend outward from body 32 further than the connector 32e. Flange 32g can inhibit scoop 50 from moving (for example, pivoting) when connector 56 is positioned within connector 32e.

FIG. 8F illustrates a cross-section taken through a portion of nasal cannula manifold 30 shown in FIG. 8C. Nasal cannula manifold 30 can be configured to allow gases (for example, oxygen) to be delivered from a gas supply tube 18 to a subject's nostril or nostrils and to allow gases exhaled from the subject's nostril or nostrils to be directed to gas sampling tube 8. Nasal cannula manifold 30 (for example, body 32) can include an interior portion 40 in fluid communication with gas delivery tube 18 (when connected to nasal cannula manifold 30), arm 34, and/or nasal prong 32a. Accordingly, delivery gases can flow through tube 18, arm 34, interior portion 40, and outward towards a nostril of the subject via nasal prong 32a. Nasal cannula manifold 30 can include an interior portion 42 that is separated from interior portion 40 by an inner wall 33. Interior portion 40 may be referred to as a first interior portion of nasal cannula manifold 30 and interior portion 42 may be referred to as a second interior portion of nasal cannula manifold 30. Interior portion 42 can be in fluid communication with opening 32f, connector 32e, nasal prong 32b, arm 36, and tube 8 when tube 8 is connected to nasal cannula manifold 30. Nasal prong 32b can receive gases exhaled from a nostril of the subject and direct such gases to interior portion 42. In some implementations, nasal cannula manifold 30 includes an inner wall 33, and in such implementations, inner wall 33 can prevent fluid communication between interior portion 40 (and nasal prong 32a, arm 34, and/or tube 18) and interior portion 42 (and opening 32f, connector 32e, nasal prong 32b, arm 36, and/or tube 8). Such configuration can reduce mixing of delivered and exhaled gases and allow for accurate measurements based on the exhaled gases.

FIG. 9A-9D illustrate another implementation of a bite block assembly 1′. Bite block assembly 1′ can be similar or identical to bite block assembly 1 in some or many respects. With reference to FIG. 9A, bite block assembly 1′ can include bite block 100, strap 3, tubes 2, 4, connectors 2a, 14, coupler 10, nasal cannula manifold 30, nasal prongs 32a, 32b, tube 8, and scoop 50 each of which is described elsewhere herein. Instead of coupler 12 and branched connector 16, bite block assembly 1′ can include branched connector 16′. Further, instead of separate tubes 6 and 22 that can supply delivery gas to bite block 100 (and additionally or alternatively to nasal cannula manifold 30), bite block assembly 1′ can include a single tube 22′ that can supply delivery gas to bite block 100. Assembly 1′ can include a nasal cannula assembly 15′ that is similar to nasal cannula assembly 15 in some or many respects. Nasal cannula assembly 15′ can include a tube 18′ that can be similar or identical to tube 18 discussed elsewhere herein. Nasal cannula assembly 15′, which can include branched connector 16′, coupler 10, tubes 8, 18, nasal cannula manifold 30, prongs 32a, 32b, tubes 2, 4, and connectors 2a, 14, can be separatable from bite block 100 and tube 22′, for example, via branched connector 16′.

Similar to branched connector 16, branched connector 16′ can allow gases from a gas source to be split between tube 18′ (for delivery to the nasal cannula manifold 30) and a gas delivery tube 22′ that can be connected to a portion of the bite block 100 for delivery of such gases into the subject's mouth. Branched connector 16′ and tubes 18′, 22′ can be similar or identical to branched connector 16 and tubes 18, 22 described above with reference to nasal cannula assembly 15. As shown, branched connector 16′ can be positioned near or above coupler 10 such that branched connector 16′ is coupled with gas delivery tube 2 and gas sampling tube 4, in contrast to branched connector 16 that is illustrated as being disposed between tubes 6, 18, and 22 (see FIGS. 1A and 1D). Gas delivery tubes 18′, 22′ can be sized to accommodate the alternate positioning of branched connector 16′. Tube 22′ can be permanently or removably connected to bite block 100. For example, tube 22′ can be positioned within recess 111 and/or gas delivery opening 110 of bite block 100 in a similar or identical manner as that described elsewhere herein with respect to tube 22.

FIGS. 9B-9D illustrate enlarged views of branched connector 16′, coupler 10, portions of tubes 2, 4, 8, 18′, and a connector 20′ coupled to an end of tube 22′. Branched connector 16′ can include a first branch 16a′, a second branch 16b′, and a third branch 16c′. First branch 16a′, a second branch 16b′, and a third branch 16c′ can be similar or identical to first branch 16a, a second branch 16b, and a third branch 16c in some, or many respects. Branch 16a′ can be permanently or removably connected to tube 2 and/or branch 16b′ can be permanently or removably connected to tube 18′ and/or tube 8. In some implementations, coupler 10 is included in nasal cannula assembly 15′. However, in alternative implementations, coupler 10 is not included. Branch 16c′ can be configured to removably connect to gas delivery tube 22′, for example, via connector 20′ secured to an end of tube 22′. Connector 20′ can be configured to secure to branch 16c′ via a snap fit engagement. Alternatively, connector 20′ can secure to branch 16c′ via a threaded engagement. Connection between connector 20′ and branch 16c′ can facilitate fluid communication between tube 22′ and tube 2, thereby allowing gases (for example, oxygen) to be delivered by tube 2 and branch 16c′ to tube 22′ (and to gas delivery channel 110 of bite block 100). Branch 16b′ can facilitate fluid communication between tube 18′ and tube 2. Branch 16a′ can facilitate fluid communication between tube 8 and tube 4. Branched connector 16′ can include an interior defined by interiors of branches 16a′, 16b′, 16c′. Branched connector 16′ can include a main body from which branch 16c′ extends (for example, at an angle), and such main portion can be bifurcated into a first portion that is in fluid communication with tubes 2, 18′ and a second portion that is in fluid communication with tubes 4, 8. Such first and second portions of such main body can be separated from one another.

As shown in FIGS. 9B-9D, a cap 24′ can be secured to branched connector 16′. FIG. 9B shows tube 22′ and connector 20′ attached to branch 16c′, FIG. 6C illustrates tube 22′ and connector 20 unattached to branch 16c′, and FIG. 9D illustrates tube 22′ and connector 20 unattached to branch 16c′ and cap 24′ in a closed state. Cap 24′ can be secured to a portion of branch 16c′ to enable a fluid flow path through branch 16c′ to be closed when connector 20′ and tube 22′ are not connected to branch 16c′. Cap 24′ can include a base 24a′ secured to (for example, around) branch 16c′, a lid 24c′ (which may also be referred to as a “closure portion”), and a strap 24b′ positioned between and connecting base 24a′ and lid 24c′. Strap 24b′ can be flexible to allow lid 24c′ to move relative to base 24a′. In some implementations, cap 24′ (for example, base 24a′) is permanently secured to branched connector 16′ (for example, to branch 16c′). FIG. 9C illustrates cap 24′ in an open position where branch 16c′ is in fluid communication with the ambient environment when not connected with tube 22′ (via connector 20′). In some implementations, a portion of connector 20′ is inserted into branch 16c′ when connected thereto. In some implementations, connector 20′ is a male luer connector and branch 16c′ includes a female luer connector. In some implementations, such luer connectors are threaded. FIG. 9D illustrates cap 24′ in a closed position, where branch 16c′ is not in fluid communication with the ambient environment. With reference to FIG. 9C, in some implementations, cap 24′ includes a plug 24d′ sized and/or shaped to fit and/or secure within branch 16c′ (for example, an opening into an interior defined within branch 16c′). Such connection of plug 24d′ within branch 16c′ can be a friction fit arrangement, for example.

The bite block assemblies, bite blocks, nasal cannula assemblies, and/or components thereof disclosed herein can be utilized with monitoring devices that can provide capnography and/or anesthetic gas measurements. For example, the block assemblies, bite blocks, nasal cannula assemblies, and/or components thereof disclosed herein can be utilized with a gas analyzer such as ISA™ gas analyzers and/or Root® with ISA™ CO₂Capnography which are commercially sold by Masimo Corporation. As another example, in some implementations, connector 14 (described above) can connect to a port in a monitoring device that provides capnography and/or anesthetic gas measurements based on the exhaled gas that is directed by the bite block 100 and/or nasal cannula assembly 15 to connector 14 by way of tube 8 and/or tube 4 (in addition to other structure of bite block 100 and/or nasal cannula assembly 15 as described in more detail elsewhere herein).

Additional Considerations and Terminology

Although this disclosure has been described in the context of certain examples, it will be understood by those skilled in the art that the present disclosure extends beyond the specifically disclosed examples to other alternative examples and/or uses of the disclosure and obvious modifications and equivalents thereof. In addition, while a number of variations of the disclosure have been shown and described in detail, other modifications, which are within the scope of this disclosure, will be readily apparent to those of skill in the art based upon this disclosure. It is also contemplated that various combinations or sub-combinations of the specific features and aspects of the examples may be made and still fall within the scope of the disclosure. Accordingly, it should be understood that various features and aspects of the disclosure can be combined with or substituted for one another in order to form varying modes of the disclosed.

Features, materials, characteristics, or groups described in conjunction with a particular aspect, or example are to be understood to be applicable to any other aspect, or example described in this section or elsewhere in this specification unless incompatible therewith. All of the features disclosed in this specification (including any accompanying claims, abstract and drawings), and/or all of the steps of any method or process so disclosed, may be combined in any combination, except combinations where at least some of such features and/or steps are mutually exclusive. The protection is not restricted to the details of any foregoing examples of devices or systems. The protection extends to any novel one, or any novel combination, of the features disclosed in this specification (including any accompanying claims, abstract and drawings), or to any novel one, or any novel combination, of the steps of any method or process so disclosed.

Furthermore, certain features that are described in this disclosure in the context of separate implementations can also be implemented in combination in a single implementation. Conversely, various features that are described in the context of a single implementation can also be implemented in multiple implementations separately or in any suitable subcombination. Moreover, although features may be described above as acting in certain combinations, one or more features from a claimed combination can, in some cases, be excised from the combination, and the combination may be claimed as a subcombination or variation of a subcombination.

Moreover, while operations may be depicted in the drawings or described in the specification in a particular order, such operations need not be performed in the particular order shown or in sequential order, or that all operations be performed, to achieve desirable results. Other operations that are not depicted or described can be incorporated in the example methods and processes. For example, one or more additional operations can be performed before, after, simultaneously, or between any of the described operations. Further, the operations may be rearranged or reordered in other implementations. Those skilled in the art will appreciate that the actual steps taken in the processes illustrated and/or disclosed may differ from those shown in the figures. Depending on the system, certain of the steps described above may be removed, others may be added. Furthermore, the features and attributes of the specific examples disclosed above may be combined in different ways to form additional examples of systems, all of which fall within the scope of the present disclosure. Also, the separation of various system components in the implementations described above should not be understood as requiring such separation in all implementations, and it should be understood that the described components and systems can generally be integrated together in a single product or packaged into multiple products.

Conditional language used herein, such as, among others, “can,” “could,” “might,” “may,” “e.g.,” and the like, unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain features, elements, and/or steps are optional. Thus, such conditional language is not generally intended to imply that features, elements, and/or steps are in any way required or that one or more embodiments necessarily include logic for deciding, with or without other input or prompting, whether these features, elements, and/or steps are included or are to be always performed. The terms “comprising,” “including,” “having,” and the like are synonymous and are used inclusively, in an open-ended fashion, and do not exclude additional elements, features, acts, operations, and so forth. Also, the term “or” is used in its inclusive sense (and not in its exclusive sense) so that when used, for example, to connect a list of elements, the term “or” means one, some, or all of the elements in the list. Further, the term “each,” as used herein, in addition to having its ordinary meaning, can mean any subset of a set of elements to which the term “each” is applied.

Conjunctive language such as the phrase “at least one of X, Y, and Z,” unless specifically stated otherwise, is otherwise understood with the context as used in general to convey that an item, term, etc. may be either X, Y, or Z. Thus, such conjunctive language is not generally intended to imply that certain embodiments require the presence of at least one of X, at least one of Y, and at least one of Z.

Language of degree used herein, such as the terms “approximately,” “about,” “generally,” and “substantially” as used herein represent a value, amount, or characteristic close to the stated value, amount, or characteristic that still performs a desired function or achieves a desired result. For example, the terms “approximately”, “about”, “generally,” and “substantially” may refer to an amount that is within less than 10% of, within less than 5% of, within less than 1% of, within less than 0.1% of, and within less than 0.01% of the stated amount. As another example, in certain embodiments, the terms “generally parallel” and “substantially parallel” refer to a value, amount, or characteristic that departs from exactly parallel by less than or equal to 10 degrees, 5 degrees, 3 degrees, or 1 degree. As another example, in certain embodiments, the terms “generally perpendicular” and “substantially perpendicular” refer to a value, amount, or characteristic that departs from exactly perpendicular by less than or equal to 10 degrees, 5 degrees, 3 degrees, or 1 degree.

While the above detailed description has shown, described, and pointed out novel features, it can be understood that various omissions, substitutions, and changes in the form and details of the devices or systems illustrated can be made without departing from the spirit of the disclosure. As can be recognized, certain portions of the description herein can be embodied within a form that does not provide all of the features and benefits set forth herein, as some features can be used or practiced separately from others. The scope of certain embodiments disclosed herein is indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.

BITE BLOCK AND ASSEMBLIES INCLUDING SAME

Information

Publication Number

Date Filed

Date Published

Inventors

Original Assignees

CPC

International Classifications

Abstract

Description

Claims

INCORPORATION BY REFERENCE TO ANY PRIORITY APPLICATIONS

Provisional Applications (1)