The present technology relates to the field of respiratory devices having nasal air intake members.
For a multitude of respiratory ailments, such as, but not limited to, snoring and sleep apnea, the utilization of various ventilation techniques may be implemented for the transmission of oxygen and/or other gases from the nostrils to a patient's upper airway so as to aid with inhalation and exhalation. Continuous positive air pressure (CPAP), or a variation thereof, is an example of such a regimen.
This Summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This Summary is not intended to identify key or essential features of the claimed subject matter, nor is it intended to be used as an aid in determining the scope of the claimed subject matter.
In an embodiment, a respiratory shield is disclosed. The respiratory shield is sized to be coupled with a respiratory device having a nasal air intake member so as to be positioned along an oral airflow axis.
Additionally, in one embodiment, a respiratory shield is disclosed, wherein the respiratory shield may include or comprise a base member, an airflow resistor, and a rigid extension associated with the airflow resistor and the base member. The respiratory shield may also include or comprise a force exerting member associated with the base member and the rigid extension, wherein the force exerting member is positioned to exert a force on the rigid extension in a direction toward the airflow resistor.
Moreover, in accordance with an embodiment, a respiratory device is disclosed. The respiratory device may include or comprise a nasal air intake member, and a respiratory shield associated with the nasal air intake member so as to be positioned to resist a degree of airflow through an oral cavity when the nasal air intake member is positioned to direct airflow into a nasal cavity.
The accompanying drawings, which are incorporated in and form a part of this specification, illustrate embodiments of the present technology, and, together with the Detailed Description, serve to explain principles discussed below.
The drawings referred to in this description are not to be understood as being drawn to scale except if specifically noted, and such drawings are only exemplary in nature.
Reference will now be made in detail to embodiments of the present technology, examples of which are illustrated in the accompanying drawings. While the present technology will be described in conjunction with various embodiments, these embodiments are not intended to limit the present technology. Rather, the present technology is to be understood as encompassing alternatives, modifications and equivalents, which may be included within the spirit and scope of the various embodiments as defined by the appended claims.
Moreover, in the following Detailed Description numerous specific details are set forth in order to provide a thorough understanding of the present technology. However, the present technology may be practiced without these specific details. In other instances, well-known methods, procedures, components, circuits and devices have not been described in detail so as to not unnecessarily obscure aspects of the exemplary embodiments presented herein.
Furthermore, the term “air” as used herein shall not be limited to any particular gaseous substance. Indeed, the term “air” is meant to refer to any gaseous substance, which may or may not be a mixture of different types of gases.
Overview
In an exemplary scenario, sleep apnea patients, as well as other respiratory patients, may utilize various types of positive air or gaseous pressure systems such as, but not limited to, CPAP, variable positive air pressure (VPAP), bi-level positive air pressure (BIPAP), and automatic positive air pressure (APAP) oxygen generators or ventilators. However, when utilizing such a system, the effectiveness of the respective treatment may suffer if the air that enters through a patient's nostrils escapes through the patient's mouth, rather than entering into the lungs.
An embodiment of the present technology provides a device that can be incorporated into the design of various nasal interfaces, or other oxygen/gas delivering type interfaces, so as to prevent the air that enters through a patient's nostrils from escaping through the patient's mouth. In particular, and to increase the effectiveness of such a treatment, the patient's mouth is closed, sealed or partially sealed so that the pressurized air or gas being delivered into the patient's nostrils for the aforementioned purpose, or for other purposes, does not “short-circuit” outward through the patient's opened mouth.
To illustrate, and in accordance with an embodiment, a respiratory shield is coupled with a respiratory device (e.g. a snoring device). The respiratory shield is sized, and positioned relative to the respiratory device, such that the respiratory shield is configured to be worn outside the mouth, and such that the respiratory shield is configured to seal off a patient's mouth area, either partially (e.g., due to vents, holes or pores defined in the respiratory shield) or completely. Indeed, the respiratory shield may be conformable to a patient's lips so as to efficiently function to restrict airflow through the patient's mouth. Furthermore, the respiratory shield may be configured to be either removable or permanently affixed to a CPAP interface.
It is noted that the present technology has significant utility in the relevant art. For many sleep apnea patients, and for other respiratory patients, who use respiratory devices when sleeping, while opening their mouths, the utilization of a respiratory shield that is worn outside the mouth and is conformable to the user's lips significantly increases the effectiveness of the treatment. Indeed, a respiratory shield as described herein may also be implemented in conjunction with a dental appliance to reduce a patient's snoring.
In addition to the foregoing, an embodiment of the present technology relates to the emission of saliva, and the subsequent absorption thereof, during the utilization of respiratory devices such as, but not limited to, snoring aids and sleep apnea products. In particular, although a non-absorbent mouth shield may be utilized, in many instances during open mouth breathing, with the use of a non-absorbent mouth shield, there is excess salivation and drooling by the patient. Accordingly, absorbent materials, such as, but not limited to, super high absorbing materials of the type utilized in infant diapers and incontinence products, are implemented as or in conjunction with the mouth shield component so that saliva may be absorbed without undue discomfort to the patient.
Various exemplary embodiments of the present technology will now be discussed. It is noted, however, that the present technology is not limited to these exemplary embodiments, and that the present technology also includes obvious variations of the exemplary embodiments and implementations described herein.
Exemplary Structures
With reference now to
It is noted that airflow resistor 111 may be constructed, for example, of soft resilient molded silicone or a hard plastic shell. However, other materials for airflow resistor 111 may also be implemented. Indeed, the present technology is not limited to any particular material for airflow resistor 111 (or any other components described herein).
Pursuant to one embodiment, however, airflow resistor 111 is configured to enable an amount of air to escape from a patient's mouth. To illustrate, an example provides that airflow resistor 111 is substantially flat or non-conforming to the shape of a patient's mouth, such as shown in
The foregoing notwithstanding, it is noted that although airflow resistor 111, which may be porous or non-porous, is shown in
To illustrate, and with reference now to
It is noted that airflow resistor 111 may also be constructed of a material capable of increasing a patient's comfort level when airflow resistor 111 is held next to a patient's mouth. Consider the example where airflow resistor 111 has no, or extremely minimal, absorption capabilities such that saliva tends to accumulate within respiratory shield 110 while the patient sleeps. This saliva may then escape downward onto the patient's chin causing significant discomfort and skin irritation. Therefore, in one embodiment, airflow resistor 111 includes a liquid absorbent material, which may be beneficial, for example, so as to absorb saliva that seeps out of a patient's mouth when airflow resistor 111 is positioned adjacent thereto.
Furthermore, although airflow resistor 111 may be generally rigid, an embodiment provides that airflow resistor 111 is constructed of an absorbent material capable of absorbing a degree of force such as to provide, for example, a cushioning effect when airflow resistor 111 is pressed against the patient's face which can increase a patient's comfort level. Similarly, in accordance with one embodiment, although airflow resistor 111 may or may not itself be generally rigid, an absorbent material 390 is coupled with airflow resistor 111 such that a similar cushioning effect may be achieved. Moreover, pursuant to one embodiment, absorbent material 390 is a liquid absorbent material configured to absorb an amount of liquid, such as sweat and saliva emitted by a patient.
Moreover, an exemplary implementation provides that a non-water-soluble lubricant, such as Vaseline™, may be implemented to enhance the seal between respiratory shield 110 and a patient's lip region, so as to minimize saliva drip and skin chafing. This lubricant may be supplied within infused disposable pads, such as within absorbent material 390, wherein these pads may be coupled with airflow resistor 111, such as by an adhesive or a fastening member (not shown), such as Velcro™, and replaced during subsequent uses (e.g., nightly) of respiratory shield 110.
Thus, various embodiments provide a device configured to reduce or eliminate the accumulation of sweat and saliva, so as to minimize the discomfort experienced by respiratory patients, through the utilization of materials that have the capability of absorbing moisture. As noted above, respiratory shield 110 may be completely constructed of absorbent materials or utilized in combination with absorbent materials, wherein these materials may be, for example, “high-absorption” and “super-absorbent” materials that “suck up” the saliva, such as due to the natural absorbent characteristics of these materials and the natural viscosity of the liquids at issue. The following are examples of “super-absorbent” materials that may be implemented: Luquafleece™, Gelok™, Gelok™ with a foam laminate, and hydrophilic Ester Foam™. However, these materials are not to be understood as encompassing all possible “super-absorbent” materials.
With reference still to
The foregoing notwithstanding, it is noted that airflow resistor 111 absorbent material 390 and seal 210 are shown in
With reference now to
Moreover, in one embodiment, a secondary shield 112 extends from, or is integrated with or within, airflow resistor 111. For example, secondary shield 112 may be positioned to function as a lower lip cover so as to collect saliva and/or divert saliva back into a patient's mouth. However, similarly to extension 370, it is noted that secondary shield 112 is an optional component, and that various embodiments of the present technology may therefore be practiced without such a component.
With reference now to
As shown in
The foregoing notwithstanding, it is noted that other implementations of a dental anchor may also be implemented, and that the present technology is not limited to the specific configuration shown in
With reference now to
To further illustrate, and with reference still to
Thus, an embodiment provides that respiratory device 310, which includes nasal air intake member 311, either includes or is integrated with respiratory shield 110, wherein respiratory shield 110 is coupled with and extends from nasal air intake member 311, and wherein respiratory shield 110 is positioned relative to nasal air intake member 311 so as to resist a degree of airflow through oral airflow cavity 340 when nasal air intake member 311 is positioned to direct airflow into nasal cavity 330. It is noted that respiratory shield 110 may be permanently coupled with nasal air intake member 311. In one embodiment, however, a removable shield is provided, wherein respiratory shield 110 is configured to be removed from, and subsequently reattached to, respiratory device 310.
It is noted that the present technology is not limited to any particular type of respiratory device or nasal air intake member. For example, as shown in
Moreover, and notwithstanding the exemplary configuration shown in
Furthermore, it is noted that placing an air seal inside a patient's mouth, behind the patient's lips, may cause a degree of discomfort during sleep. In particular, such discomfort may result, for example, from a foreign object being placed behind the patient's lips that is large enough to prevent air flow through the patient's mouth cavity. In one embodiment, however, a respiratory shield as described herein is sized so as to be worn outside a patient's mouth so as to increase a patient's level of comfort, such as shown in
With reference now to
In one embodiment, upper and lower straps 441, 442 and a fastening member 450 are included, wherein fastening member 450 is configured to fasten a number of the straps together, such as to secure first exemplary respiratory apparatus 400 around a patient's head. Furthermore, an adjusting unit 460, which may include a fitting dial, may be provided to adjust a length of one or more of the straps, such as to tighten or loosen upper straps 441 when they are fastened together.
With reference now to
With reference now to
The foregoing notwithstanding, it is noted that while various exemplary embodiments discussed herein include a respiratory device having a contoured mask, the present technology is not limited to any particular type of respiratory device. For example, and with reference now to
With reference now to
Additionally, fourth exemplary respiratory apparatus 1400 further includes a base member 720, which is coupled with extension 370. Additionally, first and second clamps or coupling members 730, 731 are implemented to respectively couple first and second hoses 351, 352 to base member 720. Furthermore, first and second hollow nasal plugs 711, 712 are respectively coupled to first and second hoses 351, 352, wherein first and second hollow nasal plugs 711, 712 may be respectively fitted in different nostrils of a patient when fourth exemplary respiratory apparatus 1400 is worn. In this manner, first and second hoses 351, 352 are coupled with first and second hollow nasal plugs 711, 712 such that fourth exemplary respiratory apparatus 1400 is configured to route air provided by an air supply (not shown) to a patient simultaneously through multiple air channels.
With reference still to
The foregoing notwithstanding, it is noted that other configurations may also be implemented, and that the present technology is not limited to the embodiment shown in
Moreover, an embodiment provides that extension 370 is an optional component, such as where base member 720 is coupled directly to either airflow resistor 111 or dental anchor 380. Therefore, various embodiments of the present technology may be practiced without the implementation of such an extension member.
Furthermore, in one embodiment, base member 720 is an optional component. Consider the example where first and second hoses 351, 352 are coupled to either airflow resistor 111 or dental anchor 380, such as by being affixed thereto by first and second clamps or coupling members 730, 731 (see, e.g.,
With reference now to
With reference now to
With reference still to
To illustrate, in an embodiment, an optional force exerting member 940 is coupled with both base member 720 and rigid extension 930, wherein force exerting member 940 is configured to exert a force on rigid extension 930 in a direction toward airflow resistor 111. In this manner, airflow resistor 111 may be automatically moved along oral airflow axis 320. Moreover, and with reference again to
The foregoing notwithstanding, it is noted that the present technology is not limited to any particular type of force exerting member. For example, force exerting member 940 may include a spring or an elastic element. Alternatively, other types of force exerting members may be implemented.
With reference now to
It is noted that respiratory device 310 includes contoured mask 312, wherein cushion 410 is implemented such as to increase a degree of comfort associated with respiratory device 310. However, the present technology is not limited to any particular type of mask. Indeed, other types of masks may also be implemented.
With reference now to
The foregoing notwithstanding, an exemplary implementation provides that airflow resistor 111 is adjustable horizontally and/or vertically. Consider the example where airflow resistor 111 is moveably coupled with base member 720, such as previously explained, but wherein adjustable respiratory shield 910 is also moveably coupled with respiratory device 310. In this manner, airflow resistor 111 may be positioned along oral airflow axis 320 irrespective of a patient's unique physical size and shape, and consequently, the same device may be utilized by patients of different sizes and shapes (e.g., youths and adults).
With reference now to
In one embodiment, sixth exemplary respiratory apparatus 1500 also includes dental anchor 380 (as shown), which is positioned to anchor with a patient's upper dental jaw region. When a patient's mouth is opened, airflow resistor 111 is positioned to block a degree of airflow through the patient's mouth. As a result, the patient is discouraged from breathing through the mouth, and therefore instead breaths through a nasal cavity.
The foregoing notwithstanding, it is noted that other implementations of a dental anchor may also be implemented, and that the present technology is not limited to the specific configuration shown in
With reference now to
In an embodiment, airflow resistor 111 is moveably coupled with vertical base member 371. In particular, a number of force exerting members 940 are coupled with both airflow resistor 111 and vertical base member 371, wherein force exerting members 940 are configured to push airflow resistor 111 in a direction away from vertical base member 371. In this manner, airflow resistor 111 may be pushed toward a patient's mouth when dental anchor 380 is anchored with a patient's jaw.
In one embodiment, an absorbent material 390 is coupled with airflow resistor 111. Absorbent material 390 may be configured to absorb a degree of force so as to provide, for example, a degree of comfort to a patient when airflow resistor 111 is pressed against the patient's face. Additionally, an embodiment provides that absorbent material 390 is a liquid absorbent material configured to absorb an amount of liquid, such as sweat and saliva emitted by a patient.
Thus, in an embodiment, adjustable respiratory shield 910 incorporates a CPAP dental appliance, which fits onto the patient's upper dental arch, with a mouth shield contained with a resilient member to maintain comfortable pressure against the open mouth area. The mouth shield may have some degree of porosity or no porosity, depending on whether a controlled degree of airflow through the device may be beneficial to the treatment.
The foregoing notwithstanding, an embodiment provides that adjustable respiratory shield 910 does not include dental anchor 380. Consider the example where extension 370 is coupled with a respiratory device while vertical base member 371 is attached to extension 370 rather than to dental anchor 380. It is therefore noted that dental anchor 380 is an optional component that may or may not be implemented.
With reference now to
With reference now to
In one embodiment, adjustable respiratory shield 910, such as shown in
It is noted that various embodiments of the present technology may be implemented without certain components discussed herein. For example, and as previously discussed, extension 370 is an optional component that may be excluded from a device fabricated in accordance with various principles described herein. Additionally, base member 720 is also one such optional component. For purposes of illustration, an exemplary arrangement will now be described in which these two optional components are excluded, although the present technology is not limited to the following arrangement.
With reference now to
Summary Concepts
It is noted that the foregoing discussion has presented at least the following concepts:
1. A respiratory shield sized to be coupled with a respiratory device having a nasal air intake member so as to be positioned along an oral airflow axis.
2. The respiratory shield of Concept 1, wherein the respiratory shield is sized to be coupled with the respiratory device so as to be positioned along the oral airflow axis when the nasal air intake member is positioned to inject air into a nasal cavity.
3. The respiratory shield of Concept 1, wherein the respiratory shield is sized to be coupled with the respiratory device so as to be positioned adjacent to an opening of an oral cavity and resist a degree of airflow through the oral cavity when the nasal air intake member is positioned to direct airflow into a nasal cavity.
4. The respiratory shield of Concept 1, including or comprising:
an airflow resistor sized to be applied against a lip region of an oral cavity, outside of the oral cavity, within a preselected pressure range when the respiratory shield is coupled with the respiratory device and the nasal air intake member is positioned to direct airflow into a nasal cavity.
5. The respiratory shield of Concept 4, wherein the airflow resistor is porous.
6. The respiratory shield of Concept 4, further including or comprising:
a liquid absorbent material coupled with the airflow resistor.
7. The respiratory shield of Concept 4, wherein the airflow resistor includes or comprises a liquid absorbent material.
8. The respiratory shield of Concept 4, further including or comprising:
an air seal coupled with the airflow resistor.
9. The respiratory shield of Concept 1, including or comprising:
a base member; and
an airflow resistor assembly moveably coupled with the base member so as to be moveable along the oral airflow axis when the respiratory shield is coupled with the respiratory device and the nasal air intake member is positioned to direct airflow into a nasal cavity.
10. The respiratory shield of Concept 9, wherein the airflow resistor assembly includes or comprises:
an airflow resistor;
a rigid extension coupled with the airflow resistor and moveably coupled with the base member; and
a force exerting member coupled with the base member and the rigid extension, the force exerting member positioned to exert a force on the rigid extension in a direction toward the airflow resistor.
11. The respiratory shield of Concept 10, wherein a size of the rigid extension and a magnitude of the force are sufficient to apply the airflow resistor against a lip region of the oral cavity, outside of the oral cavity, within a preselected pressure range when the respiratory shield is coupled with the respiratory device and the nasal air intake member is positioned to direct airflow into a nasal cavity.
12. The respiratory shield of Concept 10, wherein the force exerting member includes or comprises:
a spring or an elastic element.
13. The respiratory shield of Concept 1, wherein the respiratory shield includes or comprises:
a dental anchor sized and positioned to anchor with a dental region when the respiratory shield is coupled with the respiratory device and the nasal air intake member is positioned to direct airflow into a nasal cavity.
14. A respiratory shield including or comprising:
a base member;
an airflow resistor;
a rigid extension associated with the airflow resistor and the base member; and
a force exerting member associated with the base member and the rigid extension, the force exerting member positioned to exert a force on the rigid extension in a direction toward the airflow resistor.
15. A respiratory device including or comprising:
a nasal air intake member; and
a respiratory shield associated with the nasal air intake member so as to be positioned to resist a degree of airflow through an oral cavity when the nasal air intake member is positioned to direct airflow into a nasal cavity.
16. The respiratory device of Concept 15, wherein the respiratory shield includes or comprises:
an airflow resistor coupled with the nasal air intake member and sized to be applied against a lip region of the oral cavity within a preselected pressure range when the nasal air intake member is positioned to direct airflow into the nasal cavity.
17. The respiratory device of Concept 15, wherein the respiratory shield includes or comprises:
a base member coupled with the nasal air intake member; and
an airflow resistor assembly moveably coupled with the base member so as to be moveable along an oral airflow axis when the nasal air intake member is positioned to direct airflow into the nasal cavity.
18. The respiratory device of Concept 17, wherein the airflow resistor assembly includes or comprises:
an airflow resistor;
a rigid extension coupled with the airflow resistor and moveably coupled with the base member; and
a force exerting member coupled with the base and the rigid extension, the force exerting member positioned to exert a force on the rigid extension in a direction toward the airflow resistor.
19. The respiratory device of Concept 18, wherein a size of the rigid extension and a magnitude of the force are sufficient to apply the airflow resistor against a lip region of the oral cavity within a preselected pressure range when the nasal air intake member is positioned to direct airflow into the nasal cavity.
20. The respiratory device of Concept 18, wherein the force exerting member includes or comprises:
a spring or an elastic element.
21. The respiratory device of Concept 15, wherein the respiratory shield includes or comprises:
a dental anchor sized and positioned to anchor with a dental region when the nasal air intake member is positioned to direct airflow into the nasal cavity.
Although various exemplary embodiments of the present technology are described herein in a language specific to structural features, the subject matter defined in the appended claims is not necessarily limited to the specific features described above. Rather, the specific features described above are disclosed as exemplary forms of implementing the claims.
This application claims the benefit of U.S. Provisional Application No. 61/281,280, filed on Nov. 16, 2009, and U.S. Provisional Application No. 61/338,129, filed on Feb. 16, 2010, which are incorporated herein by reference in their entirety.
Number | Name | Date | Kind |
---|---|---|---|
5720302 | Belfer | Feb 1998 | A |
5810013 | Belfer | Sep 1998 | A |
5988170 | Thomas | Nov 1999 | A |
6012455 | Goldstein | Jan 2000 | A |
6062220 | Whitaker et al. | May 2000 | A |
6571798 | Thornton | Jun 2003 | B1 |
6675802 | Thornton | Jan 2004 | B1 |
6926004 | Schumacher | Aug 2005 | B2 |
7021312 | Cannon | Apr 2006 | B2 |
7243650 | Thornton | Jul 2007 | B2 |
7406966 | Wondka | Aug 2008 | B2 |
7500480 | Matula et al. | Mar 2009 | B2 |
7658189 | Davidson et al. | Feb 2010 | B2 |
7708017 | Davidson et al. | May 2010 | B2 |
20060237017 | Davidson et al. | Oct 2006 | A1 |
20060283461 | Lubke et al. | Dec 2006 | A1 |
20070144525 | Davidson et al. | Jun 2007 | A1 |
20070186930 | Davidson et al. | Aug 2007 | A1 |
20080110469 | Weinberg | May 2008 | A1 |
20080149105 | Matula et al. | Jun 2008 | A1 |
20090114229 | Frater et al. | May 2009 | A1 |
20090120443 | Matula et al. | May 2009 | A1 |
20090145435 | White et al. | Jun 2009 | A1 |
20090277452 | Lubke et al. | Nov 2009 | A1 |
20100132717 | Davidson et al. | Jun 2010 | A1 |
Number | Date | Country |
---|---|---|
2004308536 | Jul 2005 | AU |
2006255476 | Dec 2006 | AU |
2010214658 | Sep 2010 | AU |
1901961 | Jan 2007 | CN |
1901961 | Jan 2007 | CN |
1973914 | Jun 2007 | CN |
1973914 | Jun 2007 | CN |
101214402 | Jul 2008 | CN |
101237902 | Aug 2008 | CN |
101479010 | Jul 2009 | CN |
101628142 | Jan 2010 | CN |
1973914 | Jul 2010 | CN |
1701759 | Sep 2006 | EP |
1890755 | Feb 2008 | EP |
2035094 | Mar 2009 | EP |
1701759 | Nov 2009 | EP |
2000325481 | Nov 2000 | JP |
2007516750 | Jun 2007 | JP |
2008-541955 | Nov 2008 | JP |
2009540881 | Nov 2009 | JP |
547748 | Jul 2010 | NZ |
WO 2005063328 | Jul 2005 | WO |
WO 2006130903 | Dec 2006 | WO |
WO 2007147088 | Dec 2007 | WO |
WO 2007147088 | Dec 2007 | WO |
WO 2007147088 | Aug 2008 | WO |
Number | Date | Country | |
---|---|---|---|
20110114099 A1 | May 2011 | US |
Number | Date | Country | |
---|---|---|---|
61281280 | Nov 2009 | US | |
61338129 | Feb 2010 | US |