Patent Application
20140018691
Generally, when a patient is under conscious sedation or is in any situation in which knowledge of respiratory status is useful, it may be desirable to monitor carbon dioxide levels in the exhaled air. The monitoring of carbon dioxide exhaled by a patient during various medical procedures has become the Standard of Care.
For example, on the recommendation of the American Society of Anesthesiologist's (ASA) Committee on Standards and Practice Parameters, an amendment to the ASA Standards of Basic Anesthetic Monitoring was approved in October 2011, making monitoring of exhaled carbon dioxide the Standard of Care during moderate or deep sedation. The ASA Standards state, in part, that during moderate or deep sedation. The adequacy of ventilation shall be evaluated by the continual observation of qualitative clinical signs and monitoring for the presence of exhaled carbon dioxide unless precluded or invalidated by the nature of the patient, procedure, or equipment.
In another example, the Association of Anesthetists of Great Britain and Ireland (AAGBI) released updated recommendations, in May 2011, for the use of capnography outside the operating room. The AAGBI recommendation states, in part, that continuous capnography monitoring should be used for all anesthetized patients, regardless of the airway device used or the location of the patient, for all patients whose trachea is intubated, for all patients undergoing moderate or deep sedation, including during the recovery period, and for all patients undergoing advanced life support.
In still another example, the American Heart Association (AHA) released the updated 2010 Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. The AHA Guidelines stress the critical importance of the continuous waveform capnography to assess the quality of CPR and detect the return of spontaneous circulation.
In yet another example, the American Association for Respiratory Care (AARC) also issued updated AARC Guidelines, which recommend capnography/capnometry for verification of artificial airway placement in a patient; assessment of pulmonary circulation and respiratory status of the patient; and optimization of mechanical ventilation.
In general, the monitoring of carbon dioxide exhaled by a patient can be accomplished by inserting a nasal cannula into the patient and directing a portion of the air exhaled to a suitable apparatus for measuring the carbon dioxide in the exhaled air sample. For example, a gas analyzer, such as a capnograph, can monitor the concentration or partial pressure of carbon dioxide in the exhaled air sample.
The accuracy of such a non-invasive analysis of exhaled gases depends on the ability of a sampling system to move the exhaled air sample from the patient to the gas analyzer. The waveform of the concentration of the carbon dioxide is critical for accurate analysis. The actual concentration of carbon dioxide in the exhaled air can be affected by the oxygen supply, which reduces the accuracy of the analysis of the sample by the gas analyzer.
Generally, embodiments described herein relate to methods, systems, devices, apparatuses and kits that can be used for improved fluid analysis and detection. The various methods, systems, devices, apparatuses and kits may provide improved functionality in some aspects and/or can be used with other technologies to provide added functionality.
In various embodiments, a medical device can be a monitoring device that enhances detection and accuracy of measured carbon dioxide in exhaled breath from a non-intubated patient, who may be at least one of a nose breather or a mouth breather.
Various embodiments provide an adapter for sampling exhaled breath from a patient. The adapter can comprise a flexible portion comprising an exterior surface and an interior surface, and configured to have a diameter of the exterior surface that is less than a diameter of a hole in an oxygen supply mask configured to supply oxygen to a patient. The adapter can comprise a connector coupled to one end of the flexible tube, and configured to connect to a receiving connector on at least one of another piece of tube and a gas analyzer. The adapter can also comprise a fitting or securing device around the exterior surface of the flexible portion, and configured to adjustably fasten the flexible portion through the hole in the mask, a sampling portion comprising a plurality of holes into and around a distal end portion of the flexible portion, and at least one of the plurality of holes configured to be in communication with an interior portion of the tube, and a shaped tip on the distal end of the flexible portion.
In various embodiments, a portion of the adapter can be formable and non-kinking and may be easily inserted into an artificial nasal airway, artificial oral airway, and/or deep within a nasal passage without kinking or obstructing the adapter. In various embodiments, the adapter can comprise an open and/or a closed tip and can comprise a plurality of holes or pores proximate to the tip, which allow the flow of carbon dioxide into the flexible portion to be directed to a gas analyzer.
In various embodiments, the adapter can comprise a connector, which can be compatible with standard gas sampling lines and/or gas analyzers. For example, the connector can be compatible with standard gas analyzers used in general anesthesia and/or can be compatible with gas sampling lines used with portable carbon dioxide detection monitors. In various embodiments, the adapter may be useful in at least one of intensive care units (ICU), operating rooms, oral surgery, dentistry, an emergency medical situation (in a hospital and/or pre-hospital), veterinary medicine and/or any other situation where measurement of gases may be useful or necessary. In various embodiments, the adapter can be used on any of a variety of patients, including adults, pediatrics, infants, neonates, and/or animals.
In various embodiments, the adapter may be configured to fit into or to lock firmly into one or more ventilation holes of a face mask used to provide oxygen to a patient, or any type of oxygen delivery mask. This configuration can provide a more accurate and continuous monitoring of exhaled carbon dioxide, even if a patient becomes restless and moves her head. In one embodiment, the adapter can also be employed without a mask by placing a perforated end of the tip in one of a nasal passage, or an artificial nasopharyngeal airway, or over an oral passage, or an oropharyngeal airway, and simply taping or adhering a portion of the adapter to the face of a patient. In one embodiment, the adapter can also be employed without a mask by incorporating the adapter with any nasal cannula configured to provide oxygen to a patient.
Various embodiments provide a method of sampling carbon dioxide in a portion of exhaled air from a patient. The method can comprise coupling an adapter to a tube from a gas analyzer and to an inner portion of a mask on a patient; positioning a sampling portion of the adapter into a nasal passage; monitoring carbon dioxide in a portion of exhaled air from the nasal passage; and improving detection of carbon dioxide concentration in the exhaled air from a patient.
Various embodiments provide an adapter configured to receive a portion of exhaled air from a patient. The adapter can comprise a flexible tube comprising an exterior surface and an interior surface and configured to communicate a flow of the portion of exhaled air to a gas analyzer, and a connector coupled to one end of the flexible tube, and configured to connect to a receiving connector on the gas analyzer. The adapter can also comprise a manifold coupled to a distal end of the flexible portion and configured to communicate a flow of the portion of exhaled air to the flexible portion. The adapter can comprise a first sampling portion comprising a plurality of holes in fluid communication with the flexible portion and coupled to the manifold, and a second sampling portion comprising a plurality of holes in fluid communication with the tube and coupled to the manifold. In some embodiments, the second sampling portion can be configured in a spoon-like shape comprising the plurality of holes along an inner edge of the spoon-like shape. In one embodiment, the first sampling portion can be configured for placement inside a nasal passage, and the second sampling portion may be configured for placement over a mouth.
The present disclosure will become more fully understood from the detailed description and the accompanying drawings, wherein:
The following description is merely exemplary in nature and is in no way intended to limit the various embodiments, their application, or uses. As used herein, the phrase “at least one of A, B, and C” should be construed to mean a logical (A or B or C), using a non-exclusive logical “or.” As used herein, the phrase “A, B and/or C” should be construed to mean (A, B, and C) or alternatively (A or B or C), using a non-exclusive logical “or.” It should be understood that steps within a method may be executed in different order without altering the principles of the present disclosure.
The drawings described herein are for illustration purposes only and are not intended to limit the scope of the disclosed embodiments in any way. The drawings described herein are for illustrative purposes only of selected embodiments and not all possible implementations, and are not intended to limit the scope of any of the various embodiments. It is understood that the drawings are not drawn to scale. For purposes of clarity, the same reference numbers will be used in the drawings to identify similar elements.
As used herein, a “nasal passage” can be any of a nostril, a nare, a nasopharynx, a nasal choana, or any other portion of a nasal cavity, or combinations thereof. As used herein, the term artificial nasal airway can refer to an essentially hollow device, which typically can be placed into a nasal passage, such as, for example an artificial nasopharyngeal airway.
As used herein, an “oral passage” can be any of an oropharyngeal airway when an artificial oral airway is in place, an inside of a mouth, across a mouth, any other portion of an oral cavity, or combinations thereof. As used herein, the term artificial oral airway can refer to an essentially hollow device, which typically can be placed into an oral passage, such as, for example, an oropharyngeal airway.
Embodiments herein generally relate to devices and methods useful for measuring gases from, in or near a living organism, such as a body. For example, the devices and methods can be used for monitoring gases such as carbon dioxide. Current carbon dioxide monitoring techniques and devices have a number of limitations. For example, one of the most popular carbon dioxide monitoring approaches in the spontaneously breathing patient utilizes the nasal cannula with oxygen delivery and carbon dioxide detection. These devices have been less accurate in the past due to one or more of a variety factors, including one or more of the following: 1.) The sampling of carbon dioxide is located on the nasal cannula where the oxygen is also delivered. This creates a dilution of the carbon dioxide sample especially when the patient requires higher levels of oxygen. 2.) The nasal cannula only detects nasal carbon dioxide. If patient is a mouth breather, no detection will take place. 3.) The third problem arises when the patient's ventilatory status worsens and the patient requires an artificial airway (oral or nasal) device to assist in normal breathing. The nasal cannula will not adapt to detect carbon dioxide at a time it is needed the most when an oral airway is in place. 4.) In cases where a patient requires an oxygen mask due to needing increased oxygen delivery, practitioners will purchase a nasal cannula with oxygen delivery and carbon dioxide detection with no intention of using the oxygen system. The practitioners chose the nasal cannula oxygen/carbon dioxide type only because of the cannula's carbon dioxide detection capabilities. When this happens the facility has to purchase two devices to get oxygen with a mask and FDA approved carbon dioxide detection. This can be very costly to the facility, and patient. Some embodiments provide improvements over existing technologies because the devices described herein (in some embodiments) can be releasably attached (e.g., they can be removable) and/or positioned, extended, bent, flexed, moved, etc. to meet the particular needs of a situation and or patient.
The devices and methods described herein can overcome many of the drawbacks and limitations of existing devices and methodologies. Further, the devices and methods can be used with existing methodologies and devices to overcome their limits and drawbacks. Thus, in some instances, existing technology can continue to be used along with the devices and methods described herein.
Therefore, some embodiments relate generally to devices that are referred to herein as “adapter” devices because in some embodiments, the devices can function to work with existing or other technologies. In some cases, the devices can be used to adapt existing or new technologies to overcome their drawbacks or limitations. This can provide better analysis, but also can be economically important because it allows use of existing resources and materials.
In some embodiments, the adapter devices can have a unique design allowing for improved exhaled carbon dioxide monitoring and will alleviate one or more of the above problems.
For example, in some embodiments, the design of an adapter can allow for enhanced detection of carbon dioxide due to the adapter's flexibility and adjustability with the nasal passage. The adapters can be safely placed anywhere in the nasal passageway from the edge of the nasal passageway to the deep posterior nasal passageway or anywhere in between, for example. This can allow a practitioner to adjust the level within the nasal passageway so that he or she gets the best sampling of carbon dioxide. To those skilled in the art, this is detected by observing the waveforms through capnography technology. In some embodiments, the adapter devices are safe enough to be placed deep in the posterior nasal passageway, for example, in an area known as the “choana.” The choana is a funnel shaped area between the two posterior nasal passageways. It is located where the back of nasal passages meet and opens into the nasopharynx. This space can allow for less diluted sampling of carbon dioxide due to its position closer to the trachea and thus the lungs. At present, the nasal cannulas with carbon dioxide detection measure carbon dioxide at the edge of the anterior nasal passageway furthest from the trachea, where the carbon dioxide may be more diluted with oxygen.
Also, in some embodiments, the adapters can fit to any standard oxygen mask or nasal cannula that is attached to the patient, which can allow for a more continuous, uninterrupted sampling of carbon dioxide, even when a patient becomes restless and moves her head about. Furthermore, in some embodiments, the adapter can provide versatility in monitoring sites outside of the nasal passageway, as well as within the nasal passageway. It can be used over a mouth when a patient is mouth breathing. The dual detection model allows for multiple monitoring sites (if desired), for example, in the nasal passageway, mouth, or in the mask (ambient carbon dioxide).
Additionally, in situations where ventilatory status worsens and an artificial oral or a nasal airway device is needed, the devices (e.g., adapters) can function and work with (e.g., fit into) these artificial oral or nasal airway devices to detect carbon dioxide in this real time of need, for example, during respiratory emergencies and CPR, making the detection of the return of spontaneous respiration easier. In some aspects, the adapter can interface with existing technologies without the need to buy new systems to improve the detection of carbon dioxide. The adapter can be used with standard style masks and nasal cannulas. In some aspects they also can be used by simply attaching to the face, for example by taping to the face. The devices and methods are described in detail herein.
It should be understood and appreciated that although the systems, devices/apparatuses and methods are discussed primarily in the context of carbon dioxide detection and analysis, other gases and fluids also can be analyzed, measured and/or detected, such as, for example, oxygen, nitrous oxide, nitrogen, and other such gases and combinations of gases.
According to various embodiments, an adapter, an apparatus, a device, a system and/or a method, as described herein, connecting a tube from a monitoring apparatus to an oxygen supply mask increases the accuracy of carbon dioxide detection from air exhaled from a patient. According to various embodiments, an adapter, as described herein, connecting a tube from a monitoring apparatus to an oxygen supply mask increases the accuracy of carbon dioxide detection from an oropharyngeal airway, for example, with an artificial oral airway in place. According to various embodiments, an adapter, as described herein, connecting a tube from a monitoring apparatus to an oxygen supply mask increases the accuracy of carbon dioxide detection from a nasopharynx, for example, with the artificial nasal airway in place.
According to various embodiments, an adapter, as described herein, connecting a tube from a monitoring apparatus to an oxygen supply mask increases the accuracy of carbon dioxide detection from a nasopharynx when inserted alone into a deep nasal passage or nasal choana. According to various embodiments, an adapter, as described herein, connecting a tube from a monitoring adapter to an oxygen supply mask increases the accuracy of carbon dioxide detection from ambient oral exhaled carbon dioxide when placed across the mouth/lips. According to various embodiments, an adapter, as described herein, connecting a tube from a monitoring adapter to an oxygen supply mask increases the accuracy of carbon dioxide detection from ambient nasal exhaled carbon dioxide when placed in the nare or near the shallow nare.
According to various embodiments, an adapter, as described herein, connecting a tube from a monitoring apparatus to an oxygen supply mask provides an improved waveform of carbon dioxide concentration in exhaled air from a patient. As known to those skilled in the art, an improved waveform provides a more accurate carbon dioxide concentration reading. In one embodiment, an adapter is deployable for nasopharynx carbon dioxide sampling and/or monitoring. In one embodiment, an adapter is deployable for carbon dioxide sampling and/or monitoring in the nasal choana area of a patient. In one embodiment, an adapter is deployable, when an artificial oral airway is in place, for oropharyngeal carbon dioxide sampling and/or monitoring.
In some embodiments, an adapter, as described herein, can also be deployed without an oxygen supply mask in a nasal passage or an oral opening or both, by placing a perforated end of the adapter into one of a nasal passage, an artificial nasopharyngeal airway, a nasal choana, in an area near or in an oral passage, or an artificial oropharyngeal airway and then taping a portion of the adapter to the face of a patient. In one embodiment, an adapter, as described herein, can be deployed, without an oxygen supply mask, in a nasal passage and by placing a perforated end of the adapter into a nasal choana and then taping a portion of the adapter to the face of a patient. In one embodiment, the adapter can be connected to an oxygen supply nasal cannula.
It can be appreciated by those skilled in the art, that during medical procedures involving conscious sedation or in any situation in which knowledge of respiratory status is useful, it is desirable to monitor the exhaled air stream from a patient and deliver a portion of such exhaled air stream to a proper monitoring apparatus such as a gas analyzer, mass spectrometer, or capnograph. In various embodiments, an adapter connecting a tube from a monitoring apparatus to an oxygen supply face mask can optimize the repeated samplings taken of the exhaled air stream from a patient to provide an accurate measurement of carbon dioxide levels.
In various embodiments, when an adapter is employed for monitoring carbon dioxide in a nasal passage, the adapter can be placed deep in a nasal cavity for improved nasopharynx sampling, in which the exhaled carbon dioxide may be more concentrated than in a shallow nare area, which may be near an oxygen supply region, and therefore more accurate than shallow nasal area sampling. For example, nasopharynx sampling may be typically more accurate than shallow nare area sampling due to a high flow of oxygen in the oxygen supply mask fitted on the patient, which can dilute carbon dioxide levels.
In various embodiments, when an adapter is employed for monitoring a mouth of a patient, the adapter can be placed deep in an oral passageway when an artificial oral airway is in place for oropharyngeal airway sampling in which the exhaled carbon dioxide may be more concentrated than at an ambient mouth area, which may be near an oxygen supply region, and therefore provide more accurate ambient mouth sampling. For example, oropharyngeal airway sampling may be more accurate than ambient mouth sampling due to a high flow of oxygen in the oxygen supply mask fitted on the patient. In various embodiments, the adapter can be employed for both nasopharnyx airway sampling and oropharyngeal airway sampling.
In various embodiments, the adapter does not comprise a fitting. In such embodiments, the adapter can be placed between the mask and a skin surface, which is especially advantageous when the mask does not comprise any ventilation holes. In one embodiment, the adapter can be affixed or attached or coupled to the mask with a fastener, which can be, for example, a clip, a clamp, an adhesive strip, a hook and loop connector, a vise, bracket, clasp, snap, connector, link, tie, or combinations thereof.
In various embodiments, an adapter can comprise one of a single catheter, or a dual tube catheter or a triple tube catheter. In one embodiment, a plurality of catheters allow for one or more areas of detection of carbon dioxide in exhaled breath, in any combination a health care professional deems prudent. In various embodiments, the adapter can monitor carbon dioxide in one or more of a nasal passage, an artificial nasopharyngeal airway, an oral passage, an artificial oropharyngeal airway or air within a mask. The adapter can be deployed for monitoring end-tidal carbon dioxide (ETCO2) in a non-intubated patient.
In some embodiments, an adapter, as described herein, can also be deployed without an oxygen supply mask in a nasal passage and over an oral opening or both, by placing a perforated end of the adapter in one of a nasal passage, or an artificial nasopharyngeal airway, a nasal choana, and an area near or in an oral passage, or an oropharyngeal airway. In some embodiments, a first perforated end of the adapter can be positioned into a nasal passage and a second perforated end of the adapter can be positioned near an oral passage. In one embodiment, the second perforated end is replaced by a mouthpiece. In accordance with this embodiment, the first perforated end is positioned in the nose and the mouthpiece is positioned over and/or near the mouth. In some embodiments, a portion of the adapter is taped to the face of a patient. In some embodiments, the adapter can be connected to an oxygen supply nasal cannula.
Various embodiments provide systems for sampling exhaled breath from a patient. The systems can comprise a flexible portion comprising an exterior surface and an interior surface, and configured to have a diameter of the exterior surface that is less than a diameter of a hole in an oxygen supply mask configured to supply oxygen to a patient. The system can comprise a connector coupled to one end of the flexible portion, and configured to connect to a receiving connector on at least one of another piece of tube and a gas analyzer. The system can also comprise a fitting or a multi-piece fitting around the exterior surface of the flexible portion, and configured to adjustably fasten the flexible portion through a hole, a sampling portion comprising a plurality of holes into and around a portion of the flexible portion, and at least one of the plurality of holes configured to be in communication with an interior portion of the flexible portion, and a shaped tip on the distal end of the flexible portion.
In one embodiment, the adapter can comprise soft, hollow, and/or humidity absorbent tubing. In various embodiments, the adapter can comprise an open and/or a closed tip and can comprise a plurality of holes or pores proximate to the tip, which allow the flow of carbon dioxide into the tube and directed to a gas analyzer. In one embodiment, the adapter can comprise a sensor configured to detect carbon dioxide.
In some embodiments, the adapter can further comprise at least a portion of formable tubing integrated into at least a portion of the flexible portion between the connector and the sampling portion, and the portion of formable tubing can be configured with shape memory to hold a shape formed in the portion of formable tubing. In one embodiment, the portion of formable tubing can comprise an exterior diameter essentially equal to the exterior diameter of the flexible portion and an interior diameter essentially equal to an interior diameter of the flexible portion. In some embodiments, the sampling portion can comprise an exterior diameter essentially equal to the exterior diameter of the flexible portion and an interior diameter essentially equal to or greater than an interior diameter of the flexible portion.
In some embodiments, the system can further comprise a dryer in a portion of the interior surface of the flexible portion and the dryer can be configured to remove a portion of moisture in the exhaled breath from the patient. In some embodiments, the shaped tip at the distal end of the flexible portion comprises an essentially smooth exterior surface, and comprises a gradient exterior shape from a high center point to a plurality of lower circumference points. In one embodiment, the shaped tip can comprise a weight, which can be configured to lead the tip through a nasal passage for placement of the sampling portion into the nasal passage. In one embodiment, the shaped tip can comprise one or more holes configured to be in communication with the interior portion of the flexible portion. In some embodiments, the sampling portion can be configured for placement into a portion of a nasal passage. In some embodiments, the flexible portion is configured to communicate a portion of the exhaled air to the gas analyzer, which is configured to monitor carbon dioxide concentration. In one embodiment, the connector and the fitting are integrated together.
In various embodiments, the system can comprise a y-shaped tube connecting the sampling portion to the tube and connecting a second sampling portion to the tube. In some embodiments, the system can further comprise a flexible portion integrated between at least one of the y-shaped tube and the sampling portion and between the y-shaped tube and the second sampling portion, wherein the flexible portion-can be configured with shape memory to hold a shape formed in the flexible portion. In some embodiments, the second sampling portion can be configured in a spoon-like shape comprising a plurality of holes in communication with the y-shaped tube and can be configured with the plurality of holes along an inner edge of the spoon-like shape. In some embodiments, the sampling portion can be configured for placement inside a nasal passage, and the second sampling portion can be configured for placement over a mouth.
Various embodiments provide an adapter configured to receive a portion of exhaled air from a patient. The adapter can comprise a flexible tube comprising an exterior surface and an interior surface and configured to communicate a flow of the portion of exhaled air to a gas analyzer, and a connector coupled to one end of the flexible tube, and configured to connect to a receiving connector on the gas analyzer. The adapter can also comprise a manifold coupled to a distal end of the flexible portion and configured to communicate a flow of the portion of exhaled air to the flexible portion. The adapter can comprise a first sampling portion comprising a plurality of holes in fluid communication with the flexible portion and coupled to the manifold, and a second sampling portion comprising a plurality of holes in fluid communication with the flexible portion and coupled to the manifold.
In some embodiments, the second sampling portion can comprise the plurality of holes around a hollow cylinder at an end distal to the manifold and having an exterior diameter essentially equal to the exterior diameter of the tube and an interior diameter essentially equal to or greater than an interior diameter of the tube, and can comprise a shaped tip capping the end distal from the manifold and having an essentially smooth exterior surface, and comprises a gradient exterior shape from a high center point to a plurality of lower circumference points. In some embodiments, the first sampling portion is configured for placement into a nasal passage. In some embodiments, the second sampling portion can be configured in a spoon-like shape comprising the plurality of holes along an inner edge of the spoon-like shape. In one embodiment, the first sampling portion can be configured for placement inside a nasal passage, and the second sampling portion is configured for placement over a mouth.
In some embodiments, the adapter can comprise a flexible portion integrated between at least one of the manifold and the first sampling portion and between the manifold and the second sampling portion, wherein the flexible portion is configured with shape memory to hold a shape formed in the flexible portion. In some embodiments, the flexible portion can comprise an exterior diameter essentially equal to the exterior diameter of the tube and an interior diameter essentially equal to an interior diameter of the tube. In some embodiments, at least one of the first sampling portion and the second sampling portion comprises an exterior diameter essentially equal to the exterior diameter of the tube and an interior diameter essentially equal to or greater than an interior diameter of the tube. In some embodiments, the adapter can comprise a fastener, which is configured to affix a portion of the adapter to oxygen supply nasal cannula. In one embodiment, the adapter can further comprise the oxygen supply nasal cannula.
Various embodiments provide a method of sampling carbon dioxide in a portion of exhaled air from a patient. The method can comprise coupling an adapter to a tube from a gas analyzer to an inner portion of a mask on to a patient; positioning a sampling portion of the adapter into a nasal passage; monitoring carbon dioxide in a portion of exhaled air from the nasal passage; and improving a waveform shape of carbon dioxide concentration in the exhaled air from a patient.
In some embodiments, the method can further comprise positioning a second sampling portion of the adapter over a mouth area of the patient, and monitoring carbon dioxide in a portion of exhaled air fibril the mouth area. In some embodiments, the method can further comprise bending at least a portion of the adapter into a shape and holding the shape in the adapter. In some embodiments, the method can further comprise coupling a fitting configured into the adapter into a hole in the mask. In some embodiments, the method can further comprise removing a portion of moisture in the exhaled air with a dryer configured into the adapter. In some embodiments, the method can further comprise adjusting a position of the sampling portion of the adapter in the nasal passage. In some embodiments, the method can further comprise optimizing detection of the carbon dioxide concentration in the exhaled air from the patient.
In various embodiments, an adapter comprises a unique design for improved gas sampling, for example carbon dioxide, of exhaled breath in a spontaneous breathing patient. In various embodiments, the adapter can be connected to any oxygen mask, thus connected to the patient and allowing for adjustability and flexibility of different sites for monitoring and/or detecting carbon dioxide in exhaled breath from the patient.
Referring now to
As will be appreciated by those skilled in the art, gas analyzer 130 can be any of a carbon dioxide monitor, mass spectrometer, or a capnograph. According to various embodiments, gas analyzer 130 monitors at least one of an amount and a concentration of carbon dioxide exhaled by patient 121. In one embodiment, gas analyzer 130 monitors carbon dioxide exhaled by patient 121. Gas analyzer 130 can be configured to analyze carbon dioxide exhaled by patient 121 and any other gas that is either provided to patient 121 or exhaled by patient 121.
According to various embodiments, gas analyzer 130 is coupled to mask 125 via carbon dioxide sample line 132, which is connected to adapter 100 at connector 104 and adapter 100 is interfaced with mask 125. According to various embodiments, a “medical device,” as described herein, can be the adapter, as described herein. In one embodiment, adapter 100 may be referred to as a carbon dioxide sampling line adapter. In various embodiments, an “apparatus” or a “device,” as described herein, can be an adapter, as described herein.
With reference to
In various embodiments, connector 104 can be configured to hold a line filter (not illustrated). A line filter may be employed to minimize water vapor from entering gas analyzer 130. In one embodiment, connector 104 is configured in multiple parts, for example, connector 104 may have a threaded coupling around its diameter. Access to the line filter can be accomplished by twisting connector 104 around the threaded coupling to unseat connector 104 into two parts, which surround the line filter. In one embodiment, the line filter is in a portion of tubing 105 between connector 104 and fitting 107. In some embodiments, a line filter is replaced with a portion of water absorbing tubing. In some embodiments, the function of a line filter is performed using a Nafion® gas dryer and without a line filter. In one embodiment, at least a portion of adapter 100 comprises Nafion® tubing, which is configured to absorb water in the internal surface of the tubing 105. In one embodiment, tubing 105 is configured to absorb water in the internal surface of the tubing 105.
As illustrated in
Fitting 107 can have any suitable shape or geometry, including but not limited to the geometry as depicted in the various figures. The fitting 107 can be a single member or can be multiple members with any of a number of different geometries. For example, the fitting 107 can function to releasably secure adapter 100 to a mask 125 or into place on the patient 121. It can include one or more bumps or protrusions, etc. with valleys or depressions in between that cause the device to remain connected to or in a desired position on the mask 125 or on the patient 121. For example, the bumps can have a diameter that is at least slightly larger than the diameter of the hole 126 in the mask 125 through which it passes so that added force is required for the adapter 100 to pass over and advance beyond the bump or protrusion. As such, the fitting(s) 107 can al low the adapter 100 to be secured into a desired position so that the receiving end of adapter 100 with “perforations” or holes 106 can be in the desired location (e.g., deep in the nasal or oral passageway, outside the mouth or nose, just inside the mouth or nose, etc.).
In some embodiments, flexible portion 109 is located distal to connector 104. In some embodiments, flexible portion 109 is constructed from a material which is flexible and can have enough elasticity to be bent into a position. For example, such a material can be flexible enough to bend but not crimp flexible portion 109 and in some examples may be able to keep the shape of the bend in flexible portion 109 for a period of time. Operating temperature ranges of flexible portion 109 are typically around room temperature, such as, 20° C. to 40° C. however, flexible portion 109 may have operating temperature ranges of 0° C. to 40° C. or 0° C. to 45° C., or −20° C. to 45° C. Although operating temperature ranges of flexible portion 109 are those typically used in operating rooms, flexible portion 109 can be configured to meet extreme operating temperatures, such as those that may be encountered in military hospitals, or in arctic environments, or in outer space, or in a tropical region.
In some embodiments, flexible portion 109 is constructed from a material which is both flexible and has shape memory. In one embodiment, flexible portion 109 comprises enough elasticity to be bent into a position and enough rigidity to maintain the position over a period of time. For example, such a material can be flexible enough to bend but not crimp flexible portion 109 and should be able to keep the shape of the bend in flexible portion 109 for a period of time, for example, at least 5 minutes, or at least 15 minutes, or at least 30 minutes, or at least 45 minutes, or at least an hour, or multiple hours, or 1 day, or 1 month, or multiple months, or at least a year. Operating temperature ranges of flexible portion 109 are typically around room temperature, such as, 20° C. to 40° C., however, flexible portion 109 may have operating temperature ranges of 0° C. to 40° C., 0° C. to 45° C. or −20° C. to 45° C. Although operating temperature ranges of flexible portion 109 are those typically used in operating rooms, flexible portion 109 can be configured to meet extreme operating temperatures, such as those that may be encountered in military hospitals, or in arctic environments, or in outer space, or in a tropical region.
In various embodiments, as illustrated in the Figures, flexible portion 109 is coupled to perforated tube 110. In one embodiment, flexible portion 109 and perforated tube 110 are separate components, which are at least one of mechanically, physically, and chemically attached to one another. In one embodiment, flexible portion 109 and perforated tube 110 are fused together as a continual piece. In various embodiments, adapter 100 can comprise tubing comprising, for example, PTFE, or PEEK, or Tygon, or PVC, or silicone, or KetaSpire, or Radel, or Ixef, or Nafion or any combination thereof. In one embodiment, adapter 100 comprises anti-bacterial tubing. In various embodiments, adapter 100 comprises material that has been approved by the FDA. In some embodiments, adapter 100 comprises material which can withstand sterilization at elevated temperatures. In various embodiments, adapter 100 can comprise tubing which is biocompatible. In various embodiments, adapter 100 can comprise tubing which is typically used in airways. Those skilled in the art will appreciate that choice of materials to construct adapter 100 may be determined based on any one or more of application, price, available materials, and the like.
In one embodiment, at least a portion of flexible portion 109 comprises Nafion® tubing, which is configured to absorb water in the internal surface of the tubing. In one embodiment, flexible portion 109 is configured to absorb water in the internal surface of the flexible portion 109. In one embodiment, flexible portion 109 can be moved in any direction. A standard bendable straw having a flexible portion 109 that can maintain its shape illustrates an example of one embodiment of the mechanics of operation of flexible portion 109. In one embodiment, at least a portion of flexible portion 109 can be corrugated. In one embodiment, flexible portion 109 can be concertina-type hinge between perforated tube 110 and tubing 105. As will be apparent to those skilled in the art, flexible portion 109 and tubing 105 can comprise the same material and may be indistinguishable from each other, except for the location of each of flexible portion 109 and tube 105 in adapter 100.
Perforated tube 110 comprises a plurality of holes 106 which are in communication through adapter 100 to gas analyzer 130. The term “perforated” is used herein, but should not be considered limiting, and refers to any suitable “opening” or series of openings on adapter 100 for receiving a gas that is to be analyzed. For example, the perforations can be one or more holes, slits, apertures, openings, membranes, etc. of any shape, size or number. In one embodiment, plurality of holes 106 can be a plurality of pores in a membrane which is coupled to a portion of perforated tube 110. In one embodiment, perforated tube 110 comprises tip 108, which can be hollow. In one embodiment, tip 108 is in communication through adapter 100 to gas analyzer 130. In various embodiments, at least one of plurality of holes 106 and tip 108 is configured to receive a gas exhaled by the patient 121, which can be sampled by gas analyzer 130. In one embodiment, at least one of plurality of holes 106 and tip 108 is configured to transfer carbon dioxide exhaled by patient 121 to gas analyzer 130. In one embodiment, tip 108 is closed or is solid. In one embodiment, tip 108 can comprise at least one hole 106 in a portion of tip 108, which is protected from nasal material entering holes as adapter 2100 is being pushed into nasal passage 165. For example, tip 108 may comprise a plurality of holes 106 in a surface closest to the perforated tube 110. In another example, tip 108 can be mushroom-shaped having a circumference at tip 108, which is larger than a circumference of perforated tube 110. In this example, a plurality of holes 106 can be positioned in tip 108 and be configured to communicate with gas analyzer 130. In this example, a plurality of holes 106 can be positioned in a surface of tip 108, which is closest to perforated tip 108, and be configured to communicate with gas analyzer 130.
In various embodiments, tip 108 comprises at least one of soft edges, rounded edges, and chamfered edges, which can minimize damage to tissue as adapter 100 is placed in an airway. In one embodiment, tip 108 is shaped having soft edges. In one embodiment, tip 108 is shaped having rounded edges. In one embodiment, tip 108 is shaped having chamfered edges. In one embodiment, at least one tip 108 and perforated tube 110 comprises a balloon. In one embodiment, at least one of tip 108 and perforated tube 110 is weighted, which can assist in at least one of placing the adapter 100 in an airway and keeping adapter 100 positioned in a nasal passage or an artificial oral airway while patient 121 is breathing. In some embodiments, tip 108 can be shaped having an essentially smooth exterior surface, and comprises a gradient exterior shape from a high center point to a plurality of lower circumference points. In one embodiment, tip 108 can comprise a weight, which can be configured to lead tip 108 through a nasal passage for placement of perforated tube 110 into the nasal passage. In one embodiment, the shaped tip 108 can comprise one or more holes 106 configured to be in communication with the interior portion of the perforated tube 110. In one embodiment, adapter 100 can comprise a balloon coupled to a portion of adapter 100 and configured to secure portion of adapter 100 in a nasal passage of patient 121. In one embodiment, adapter 100 can comprise a weighted member coupled to a portion of adapter 100 and configured to secure a position of adapter 100 in a nasal passage or an artificial oral airway of patient 121.
With reference to
With reference to
Now turning to
In various embodiments, fitting 107 can be any type of fitting to connect adapter 100 to mask 125 known to those skilled in the art or is developed in the future. In one embodiment, connector 104 is configured to operate as fitting 107 and couple adapter 100 to mask 125. For example, tube 105 is configured to have an outer diameter that is smaller than the diameter of holes 126, which allows tube 105 to be pushed through holes 126 from the inside of mask 125 to mate with connector 104, which is coupled to the exposed end of tube 105, thus coupling tube 105 to mask 125.
In one embodiment, fitting 107 has an annular surface on an end facing towards connector 104 and a diameter of the annular surface is larger than a diameter of one of the holes 126. In one embodiment, fitting 107 has at least one of a barbed fitting and a bayonet fitting at an end of fitting 107 facing towards flexible portion 109. For example, perforated tube 110 may be pushed through one of the holes 126 and followed by flexible portion 109 moving through one of the holes 126 until fitting 107 mates with one of the holes 126 coupling adapter 100 to mask 125. In one embodiment, fitting 107 may be pushed into one of the holes 126 allowing the end of fitting 107 facing towards flexible portion 109 to permanently couple adapter 100 and mask 125. For example, fitting 107 may be pushed into hole 126 until a barbed fitting or a bayonet fitting clips into place inside of mask 125 thereby coupling adapter 100 to mask 125. In one embodiment, fitting 107 is a tapered portion of tubing 105, which allows for a predetermined length of adapter 100 to be brought into mask 125.
In one embodiment, fitting 107 essentially locks (releasably or permanently) adapter 100 in one of the holes 126 at a certain position within mask 125. As noted, fitting 107 as depicted is one non-limiting example of a size and geometry. As noted above, the fitting 107 can be smaller or larger, and have more than one member to releasably or permanently secure or lock the adapter 100 into a desired position. In one embodiment, fitting 107 increases friction allowing adapter 100 to slide (some amount of force may be applied) into a position within mask 125 while creating enough friction to hold adapter 100 at the position within mask 125. In one embodiment, fitting 107 is permanently fixed to tubing 105, which can provide a repeatable length between fitting 107 and tip 108. In one embodiment, fitting 107 may slide along tubing 105 such that the length between fitting 107 and tip 108 may be adjusted to accommodate a variety of applications, or a variety of mask 125 types, or a variety of mask 125 sizes, or a variety of facial configurations of patient 121. In one embodiment, fitting 107 is both lockable and releasable such that length between fitting 107 and tip 108 may be adjusted to accommodate a variety of applications, or a variety of mask 125 types, or a variety of mask 125 sizes, or a variety of facial configurations of patient 121. In various embodiments, fitting 107 is configured to allow adjustability of tube 105 to place perforated tubing 110 in a targeted area of nasal passage 165, such as, for example, the nasal choana. In one embodiment, tubing 105 can be configured to have predetermined positions to lock or to releasably lock fitting 107 onto tubing 105. Typically, about 2 to about 4 inches between fitting 107 and tip 108 is a length that is useful for many applications of adapter 100. However, any length between fitting 107 and tip 108 can be used. For example, but not limited to, the length between fitting 107 and tip 108 can be 1 to 3 inches, or 1 to 5 inches, or 2 to 5 inches, or 2 to 6 inches. In some embodiments, tubing 105 comprises graduated marking configured to ensure repeatable positioning of adapter 100 within mask 125. In one embodiment, tubing 105 comprises graduated marking configured for a variety of different sizes, shapes, designs, and/or brands of mask 125 to ensure repeatable and correct positioning of adapter 100 in any of a variety of mask 125. In one embodiment, tubing 105 comprises graduated markings configured for any of a variety of different sizes, shapes, gender, species, and age groups of patients to position of adapter 100 in a targeted area of nasal passage 165, such as, for example, the nasal choana, in any of a variety of patient 121 types. In some embodiments, fitting 107 may be constructed with multiple pieces. In one embodiment, fitting 107 is integrated with connector 104, into a single piece or a group of multiple pieces.
With reference to
Turning now to
In one embodiment, nasal passage 165 in nose 160 can be a nasopharynx with the artificial nasal airway in place. In one embodiment, nasal passage 165 in nose 160 can be a nasopharynx when the artificial nasal airway is inserted alone deep into the nasopharyngeal area/space. In one embodiment, nasal passage 165 in nose 160 can be the nare or an edge of the nare. In various embodiments, when adapter 100 is employed for monitoring an artificial nasal airway, adapter 100 can be placed deep in a nasal cavity for nasopharyngeal airway sampling and/or monitoring. In various embodiments, adapter 100 can be positioned in an artificial nasal airway and then adjusted to detect carbon dioxide in any nasal-pharynx alone or within a nasopharyngeal airway.
Moving to
In
Now with reference to
Similarly, although adapter 101 is shown with two perforated tubes 110, each with a flexible portion 109, and each with a plurality of holes 106, it should be understood that in some cases, one tube can have a single hole 106 while the other has multiple holes and/or one perforated tube 110 can have the flexible portion 109 while the other does not, etc. Also, while not shown, each perforated tube 110 can feed into a single chamber with in tube 105 or into separate chambers or passageways within tube 105. As such, gases from the different locations can be separately analyzed and compared, if desired.
With attention directed to
In various embodiments, as illustrated in the Figures, each of a plurality of flexible portion 109 is coupled to one of the plurality of perforated tube 110. In various embodiments, the plurality of perforated tube 110 is in communication through adapter 115 to gas analyzer 130. In one embodiment, the plurality of perforated tube 110 is configured to transfer carbon dioxide exhaled by patient 121 to gas analyzer 130.
As illustrated in
For example, each of the plurality of perforated tube 110 may be pushed through hole 126 and followed by flexible portion 109 moving through the hole 126 until at least one fitting 107 mates within one hole 126 thereby coupling adapter 115 to mask 125. In one embodiment, at least one fitting 107 may be pushed into one hole 126 allowing the end of the at least one fitting 107 facing towards tip 108 to permanently couple adapter 115 mask 125. For example, the at least one fitting 107 may be pushed into the hole 126 until a barbed fitting or a bayonet fitting clips into place inside of mask 125 thereby coupling adapter 115 to mask 125. Although
In one embodiment, at least one fitting 107 essentially locks adapter 115 in one hole 126 at a certain position within mask 125. In one embodiment, fitting 107 increases friction allowing each of the plurality of perforated tubes 110 to slide into a position within mask 125 while creating enough friction to hold each of the plurality of perforated tubes 110 at the position within mask 125. As discussed herein, fitting 107 can be any type of fitting to connect adapter 115 to a mask 125 known to those skilled in the art or developed in the future. In one embodiment, connector 104 is configured to operate as fitting 107. For example, tube 105 is configured to have an outer diameter that is smaller than the diameter of hole 126, which allows tube 105 to be pushed through hole 126 from the inside of mask 125 to mate with connector 104, which is coupled to the exposed end of tube 105, thus coupling tube 105 to mask 125. In one embodiment, connector 104 can also function as fitting 107. In some embodiments, connector 104 has an outer diameter that is smaller than the diameter of hole 126, which allows connector 104 to be pushed through hole 126 from the inside of mask 125 to mate with sample line 132. In this embodiment, connector 134 may operate as fitting 107 or as a portion of fitting 107.
The use of multiple fittings 107, including fittings that permit securement into more than one position for each perforated tube 110 can permit each perforated tube 110 to have a desired length and positioning with respect to the patient 121. For example, one can be secured “longer” so that one perforated tube 110 can be positioned deep into the oropharyngeal airway or nasal passageway, while the other perforated tube 110 is secured “shorter” so that it can be positioned outside of the nasal passage 165 or over the oral passage 150, for example. Fittings 107 with bumps or protrusions can be used, for example, in such cases, or any other suitable orientation can be used.
In some embodiments, tubing 105 comprises graduated marking configured to ensure repeatable positioning of adapter 100 within mask 125. In one embodiment, tubing 105 comprises graduated marking configured for a variety of different sizes, shapes, designs, and/or brands of mask 125 to ensure repeatable and correct positioning of adapter 100 in any of a variety of masks 125. In one embodiment, tubing 105 comprises graduated marking configured for any of a variety of different sizes, shapes, genders, species, and age groups of patients to position an adapter 100 in a targeted area of nasal passage 165, such as, for example, the nasal choana, in any of a variety of patient 121 types.
In various embodiments, adapter 115 can be used to monitor gas exhaled by patient 121 in more than one location within mask 125. For example, adapter 115 may be positioned to be in communication with gas exhaled from patient 121 from both oral passage 150 and nasal passage 165. In another example, adapter 115 may be positioned to be in communication with gas exhaled from patient 121 from oral passage 150 and another location within mask 125. In still another example, adapter 115 may be positioned to be in communication with gas exhaled from patient 121 from nose 160 and another location within mask 125. As will be apparent to those skilled in the art, another location within the mask 125 can be a location as illustrated in
Again referring to
In one embodiment, a method of use can also include coupling adapter 115 to carbon dioxide sample line 132. In one embodiment, a method of use can also include coupling adapter 115 directly to gas analyzer 130. In one embodiment, a method of use can include collecting gas exhaled by patient 121 and transferring the gas to gas analyzer 130. In one embodiment, a method of use can include determining an amount of carbon dioxide exhaled by patient 121. In various embodiments, adapter 115 can be employed for both nasal passage sampling and/or monitoring and oral passage sampling and/or monitoring. In one embodiment, adapter 115 can be employed for both nasopharyngeal sampling and/or monitoring and oropharyngeal sampling and/or monitoring.
Moving to
Turning to
Finally, with reference to
Now moving to
In various embodiments, connector 104 is coupled to tubing 105. In some embodiments, connector 104 and tubing 105 are separate components with connector 104 configured to be seated around tubing 105. In one embodiment, connector 104 is fused to tubing 105. Also, as illustrated in the Figures, tubing 105 interfaces with fitting 107. In various embodiments, fitting 107 is configured to interface with mask 125, as described herein. However, in some embodiments, adapter 1100 does not include fitting 107. In one embodiment, connector 104 and fitting 107 are integrated into one piece, which operates both as the fitting and as the connector. At an end of tubing 105, distal to connector 104 is flexible portion 109. In one embodiment, flexible portion 109 can be moved in any direction, as discussed herein. In some embodiments, flexible portion 109 is constructed from a material which is flexible and can have enough elasticity to be bent into a position. For example, such a material can be flexible enough to bend but not crimp flexible portion 109 and in some examples such a material may be able to keep the shape of the bend in flexible portion 109 for a period of time.
In some embodiments, flexible portion 109 is constructed from a material which is both flexible and has shape memory. In one embodiment, flexible portion 109 comprises enough elasticity to be bent into a position and enough rigidity to maintain the position over a period of time. For example, such a material can be flexible enough to bend but not crimp flexible portion 109 and should be able to keep the shape of the bend in flexible portion 109 for a period of time, as discussed herein. In one embodiment, tubing 105 and/or flexible portion 109 can be configured to absorb water in the internal surface of tubing 105 and/or flexible portion 109.
In various embodiments, as illustrated in
In one embodiment, perforated tube 110 comprises tip 108, which can be hollow. In one embodiment, tip 108 is in communication through adapter 1100 to gas analyzer 130. In various embodiments, at least one of plurality of holes 106 and tip 108 is configured to receive a gas exhaled by the patient 121, which can be sampled by gas analyzer 130. In one embodiment, at least one of plurality of holes 106 and tip 108 is configured to transfer carbon dioxide exhaled by patient 121 to gas analyzer 130. In one embodiment, tip 108 is closed or is solid. As discussed herein, tip 108 can comprise at least one of soft edges, rounded edges, and chamfered edges, which can minimize damage to tissue as adapter 1100 is placed in an airway. In one embodiment, at least one tip 108 and perforated tube 110 is weighted, which in at least one of placement of adapter 1100 in an airway and keeping adapter 1100 positioned in an airway while patient 121 is breathing. In one embodiment, adapter 1100 can comprise a balloon coupled to a portion of adapter 1100 and configured to secure a portion of adapter 1100 in an airway of patient 121. In one embodiment, adapter 1100 can comprise a weighted member coupled to a portion of adapter 1100 and configured to secure a portion of adapter 1100 in an airway of patient 121.
In various embodiments, adapter 1100 comprises mouthpiece 1110. In some embodiments, mouthpiece 1110 comprises edge 1111, which may be formed to fit over the contour around oral passage 150, such as, for example, mouth, lips, and/or surrounding skin. In some embodiments, adapter 1100 can be configured in a spoon-like shape comprising a plurality of openings 1112 in communication with tubing 105. In one embodiment, adapter 1100 can be configured with a plurality of openings 1112 along inner edge 1111 of the spoon-like shape. In one embodiment, edge 1111 comprises a removable adhesive material to fasten mouthpiece 1110 over oral passage 150, such as, for example a mouth. In one embodiment, edge 1111 comprises sticky material to fasten mouthpiece 1110 over oral passage 150, such as, for example a mouth. Mouthpiece 1110 comprises a plurality of openings 1112 which is in fluid communication with tubing 105. In one embodiment, a portion of flexible portion 109 can be between tubing 105 and mouthpiece 1110. The flexible portion 109, as described herein, facilitates the positioning of mouthpiece 1110 over oral passage 150, such as, for example a mouth.
In various embodiments described herein, any perforated tube 110 can be replaced with mouthpiece 1110. For example, any embodiment comprising perforated tube 110 can comprise mouthpiece 1110 instead of perforated tube 110. In some embodiments, center area 1114 located inside of edge 1111 of mouthpiece 1110 can comprise a perforated film or perforated layer, which is in fluid communication with opening 1112 (not shown). In some embodiments, center area 1114 can have a concave shape. In some embodiments, center area 1114 can be configured in a cup-like shape. In one embodiment, the perforated film or perorated layer may further comprise a filter, which is either integrated thereto or attached thereto. In one embodiment, at least a portion of adapter 1100 is configured to absorb water in the internal surface, such as, for example, Nafion® tubing, which is configured to absorb water in the internal surface of the tubing. In one embodiment, a portion of mouthpiece 1110 is configured to absorb water in the internal surface, such as, for example, center portion 1114 and/or edge 1111.
In some embodiments, adapter 100 or adapter 1100 can be affixed to an oxygen-supply nasal cannula with fastener 175. Fastener 175 can be, for example, a clip, a clamp, an adhesive strip, a hook and loop connector, a vise, bracket clasp, snap, connector, link, tie, or combinations thereof. Fastener 175 should not crimp adapter 100 or adapter 1100, which thus can limit or eliminate flow to gas analyzer 130. Fastener 175 can be removable. In some embodiments, fastener 175 can fix adapter 100 or adapter 1100 to mask 125 for a one time use (for example, not removable). In some embodiments, for adjustability fastener 175 can movably fix adapter 100 or adapter 1100 for either mask or cannula applications. In one embodiment, adapter 1100 can be integrated into or onto an oxygen-supply nasal cannula.
Y-connector 180 can be coupled to one or more of adapter 100. Y-connector 180 can be coupled to one or more of adapter 1100. Y-connector 180 can be coupled to a combination of one or more of adapter 100 and one or more of adapter 1100. In some embodiments, Y-connector 180 comprises three different split tubings. In some embodiments, Y-connector 180 comprises four or more different split tubings. In some embodiments, at least one or more of adapter 100 and adapter 1100 can be permanently attached to Y-connector 180. In one embodiment, tubing 185 can be threaded through hole 126 in mask 125. In one embodiment, fitting 107 can lock Y-connector to mask 125. In some embodiments, at least one or more of adapter 100 and adapter 1100 can be connected to one or more connectors 1104, which are located within mask 125. In one embodiment, Y-connector 180 allows a practitioner to thread only one tube through mask 125 instead of multiple tubes through mask 125 when at least one or more of adapter 100 and adapter 1100 are employed.
However, in some embodiments, fitting 107 is not included with Y-connector 180. In such embodiments, connector 1104 can be configured to operate as both a connector and as a fitting. In such embodiments, mask 125 can be positioned between connector 1104 and Y-connector 180 for coupling adapter 100 to mask 125.
In some embodiments, adapter 100 does not comprise fitting 107. In various embodiments, adapter 100 can be placed between mask 125 and skin, as illustrated in, for example,
With reference to
Referring to
In some embodiments, one of the plurality of perforated tube 110 is positioned in nasal passage 165 and another of the plurality of perforated tube 110 is positioned over oral passage 150. In one embodiment, one of the plurality of perforated tube 110 is replaced by mouthpiece 1110. In accordance with this embodiment, one of the plurality of perforated tube 110 is positioned in nasal passage 165 and mouthpiece 1110 is positioned over oral passage 150, such as, for example a mouth. In some embodiments, perforated tube 110 extends into nasal passage 165 and is configured to be positioned above and beyond the top of the cannula 202.
Now moving to
With reference to
In various embodiments, combination tube 255 comprises oxygen portion 256 and carbon dioxide portion 258. Oxygen 205 flows from a source (not illustrated) through oxygen supply tube 253 and exits through cannula 202 to supply oxygen 205 to patient 121 through nasal passage 165. In addition, oxygen 205 flows from a source (not illustrated) through oxygen portion 256 and exits through cannula 202 to supply oxygen 205 to patient 121 through nasal passage 165. In various embodiments, the at least a portion of adapter 100 is coupled to carbon dioxide portion 258. Carbon dioxide 210 is exhaled by patient 121 and flows from the at least a portion of adapter 100 through carbon dioxide portion 258, which may be in communication with gas analyzer 130.
With reference to
With reference to
In
Now in
Finally with reference to
Some embodiments herein relate to methods and devices for analyzing a gas or fluid from a patient where a device as described herein is coupled to or attached to an existing oxygen delivery system or respiratory system, for example. Thus, some embodiments relate to conversion kits, devices and methods for converting technology to have the ability to better detect and analyze gases from a patient. In some embodiments, the devices or adapters can be attached, then removed. The devices can be secured in different positions to better fit the anatomy and situation of a given patient in that the lengths and positions are adjustable in many of the embodiments disclosed herein. The devices disclosed herein, in many aspects are bendable, flexible, adjustable, positionable and removable. Thus, the devices can be provided as kits for adapting or converting existing apparatus to have added functionality or improved functionality.
As used herein, “in one embodiment” can refer to multiple embodiments. “In one embodiment” is effectively equivalent to “in some embodiments.”
Tubes or conduits such as cannulas (i.e., cannulae) and catheters have been used for fluid and/or gas detection and analysis in many parts of the body. The nasal passage is a unique environment, however, characterized by the presence or mucus, moisture, and sometimes blood or other debris. While a nasal tube can be placed within a nasal passage of a subject so as to monitor carbon dioxide, the presence of mucus, moisture, condensation, blood, and/or other debris may clog the distal end of the tube during insertion or use, which can interfere with reliable, predictable, and accurate carbon dioxide detection. Additionally, it can be very difficult to position typical medical grade tubing into a location within the nasal passageway that allows for a precise and reproducible read-out of carbon dioxide levels of a subject. For instance, a medical professional can insert a conventional medical grade tubing into a nasal passageway of a subject so as to monitor exhaled carbon dioxide, but typically, it is difficult to position conventional tubing into a location in the nasal passageway that allows for precise and reproducible carbon dioxide measurements and during insertion and/or use nasal mucus clogs the holes or perforations at or near the distal end of the tube and/or moisture accumulates within the tubing, which skews the carbon dioxide detection by the monitor that is connected to the tubing. Accordingly, there is a need for a nasal carbon dioxide detection device that can be easily positioned within the nasal passageway of a subject (e.g., an animal, preferably a human, particularly children, and elderly patients) whereby said device is characterized by formability at the distal end of the tube (which allows for precise placement within the nasal passageway), reduced clogging of holes or perforations near the distal end of the tube, and/or features, such as a desiccant housing, which removes condensation that may accumulate during insertion or use. In several embodiments, precise placement within the nasal passageway includes placement in the nasal choanal space, the posterior nasopharynx region, and/or the nasopharynx.
Various embodiments described herein relate to a nasal tube, conduit, cannula, or catheter for monitoring end-tidal carbon dioxide levels in a patient (e.g., a human such as, an adult, a child, or an elderly person), at the nasal passage, preferably within the choana space or region (the paired openings between the nasal cavity and the nasopharynx) and methods of use thereof. Some nasal carbon dioxide detectors (e.g., nasal cannula or nasal prong style) are typically configured to detect carbon dioxide at near the exit of the nasal passage. These devices are notoriously unreliable and inaccurate for carbon dioxide measurement. It is contemplated that the monitoring of carbon dioxide using a nasal tube, conduit, cannula, or catheter placed in the choana space or region (e.g., any one or more of the devices depicted in
Capnography includes monitoring and/or measurement of the concentration or partial pressure of carbon dioxide in respiratory gases (e.g., exhaled carbon dioxide). Some capnographs measure infrared absorption in the exhaled gas, and thus, determine a level of ETCO2. The increased accuracy of some embodiments will be shown by superior waveform capnography than is typical of prior art devices. The improved waveforms can be enabled by the various methods and/or structures described herein.
A tube can be placed in a nasal passage to monitor carbon dioxide. Nasal passages sometimes have mucus or other substances that can clog the distal end of the tube, which can interfere with fluid detection and analysis in nasal passages. For example, a medical professional can insert a tube into a nasal passageway to monitor exhaled carbon dioxide. Nasal mucus can clog holes or perforations near the distal end of the tube. Increased condensation and/or clogging inside the tube can prevent accurate carbon dioxide measurements or other measurements. Thus, there is a need for a device that reduces clogging of holes or perforations near the distal end of the tube. There is also a need for a device that reduces condensation, liquid, clogging, and/or buildup of nongaseous substances inside the sampling tube. (Some embodiments are configured to remove condensation, while some embodiments are not configured to remove condensation.)
Several embodiments described herein include a collection of holes that are protected from mucus by a covering and/or by geometry that reduces the likelihood of mucus entering the holes. These embodiments can maximize the amount of gas that can enter a sampling tube, such as a sampling catheter inserted into a nasal passage to detect exhaled carbon dioxide.
In some embodiments, the protective geometry and/or covering is combined with a formable tube. A malleable wire can make a tube formable. Formability can be beneficial in many circumstances such as with insertion in deep nasal passage ways versus the upper nasal turbinates. In several embodiments, formability can help prevent injury during insertion and/or use in all patient populations, including children, the elderly, patients on blood thinning medications, and immunocompromised patients. Some tip embodiments are not formable. Many tip embodiments can be used with a formable system or without a formable system.
Any material can be used to make a catheter more formable if the material helps the catheter hold a formed shape. For example, a catheter can start in a first shape (e.g., straight) and then can be formed to a second shape (e.g., curved). The formable material can help the catheter maintain the second shape.
Some embodiments include a tip for sampling exhaled breath from a patient. The tip can include a tubular portion that has an exterior surface, an interior surface and a lumen formed by the interior surface to fluidly communicate the exhaled breath. The tip can also include a distal member coupled to the tubular portion such that at least a portion of the distal member is located distally relative to at least a portion of the tubular member. The distal member can have a distal end and a proximal end, where the distal end faces a distal direction and the proximal end faces a proximal direction. The proximal end can include at least one hole in fluid communication with the lumen. In some embodiments, the hole (or holes) on the proximal end is protected and/or shielded from mucus as the tip is inserted distally into a nasal passageway. As a result, the tip can result in superior gas analysis than would be possible with a clogged tip.
The distal member 304 can have a proximal end 316 and a distal end 320. In
In some embodiments, a tubular portion has a first outer diameter, the distal member has a second outer diameter, and the second outer diameter is larger than the first outer diameter. For example, the tubular portion 308 can have a smaller diameter than the distal member 304. In some embodiments, the maximum thickness of the tubular portion 308 is at least 10%, at least 25%, or at least 55% smaller than the maximum thickness of the distal member 304.
Several embodiments include a tip that has at least one strut that couples a tubular portion to a distal member. Some embodiments include at least two struts that couple the tubular portion to the distal member.
Some tip embodiments include a passage 344 located between the struts 340. The passage 344 can be in fluid communication with the lumen 328 of the tubular portion 308 and can be in fluid communication with the hole 336 of the proximal end 316 of the distal member 304 such that the tip 300 is configured to enable exhaled breath from a patient to enter the hole 336, then move through the passage 344, and then move through the lumen 328. Passages 344 in
The various parts of the tip, adapter, tube, and/or adapter assembly can be bonded together to form one piece and/or to make the outside smoother to facilitate insertion into a body. Bonding can prevent the pieces from coming apart. In some embodiments, the tip, adapter, tube, and/or adapter assembly are formed as one part.
The tubular portion's lumen 328 can have a central axis 350. The passages 344 can be oriented at an angle of at least eight degrees relative to the central axis. In several embodiments, the passages are oriented at an angle of at least or equal to three degrees and/or less than or equal to 15 degrees relative to the central axis; at least or equal to 10 degrees and/or less than or equal to 80 degrees relative to the central axis; and/or at least or equal to 20 degrees and/or less than or equal to 45 degrees relative to the central axis.
In some embodiments, four angled holes extend from the inner lumen proximally out of the back of the tip. The holes are protected due to their exit point on the back of the tip below the outer surface. Struts between the holes can provide support to the outer surface of the tip.
Tips can be any length. For example, a tip can be 100 cm long or 1 mm long. Some tips are between 10 cm and 0.2 cm long.
In some embodiments, tips include a dome covering such as the dome covering 306 of the distal member 304 in
Referring now to
In several embodiments, a tubular portion includes at least one passage oriented radially outward from a lumen such that the tip is configured to enable exhaled breath from a patient to enter the hole, then move through the passage, and then move through the lumen. The passage can be radially shielded by the dome covering.
In some embodiments, some holes oriented radially outward are covered by a dome while other holes oriented radially outward are not covered by the dome. Many holes can be shielded by a shielding structure, such as a dome.
In the illustrated embodiment, the passages 390 are radially shielded by the dome covering 364. In other words, the dome covering 364 at least partially blocks mucus from passing through the dome covering 364 in a radially inward direction relative to the central axis 378.
In some embodiments, the central axis 378 of the tubular portion 376 is also the central axis of the tip 360. The tip 360 can include at least one outer surface 416 that faces radially away from the central axis 378. In several embodiments, the outer surface 416 does not have holes in fluid communication with a lumen.
Referring now to
In some embodiments, a tip for sampling exhaled breath from a patient includes an at least partially flexible tube. As described previously, the tube can include a first lumen configured to communicate the exhaled breath towards a gas analyzer. The tip can also include a distal member that has a distal end and a proximal end. The distal end faces a distal direction and the proximal end faces a proximal direction. The tip can further include a tubular connector comprising a second lumen. The tubular connector can couple the distal member to the tube. The tip can also include a passage located radially between a portion of the tubular connector and a portion of the distal member.
The tube 312 comprises a first diameter, the distal member 304 comprises a second diameter, and the tubular connector 308 comprises a third diameter. In some embodiments, the third diameter is smaller than the first diameter and the third diameter is smaller than the second diameter (as illustrated in
Some embodiments include a tip for sampling exhaled breath or carbon dioxide from a patient and/or for insertion into a passage of the body, such as a nasal passage or mouth. The tip can include a first lumen comprising a proximal portion and a distal portion. The tip can also include a second lumen comprising a proximal portion, a distal portion, and an opening oriented proximally. The second lumen can be positioned radially outward from the first lumen. The tip can also include an internal passage that fluidly couples the distal portion of the first lumen to the distal portion of the second lumen such that the tip is configured to enable the exhaled breath to enter the tip at the opening of the second lumen, then move in a distal direction through the second lumen, then pass through the internal passage, and then move in a proximal direction through the first lumen towards a gas analyzer. A dome covering can be coupled around at least a portion of a lumen.
The tip 450 can also include an internal passage 510 that fluidly couples the distal portion 478 of the first lumen 462 to the distal portion 496 of the second lumen 470 such that the tip 450 is configured to enable the exhaled breath to enter the tip at the opening 500 of the second lumen 470, then move in a distal direction through the second lumen 470, then pass through the internal passage 510, and then move in a proximal direction through the first lumen 462 towards a gas analyzer (as illustrated by the dashed lines) and/or through a sampling tube, which is fluidly coupled to a gas analyzer.
In the illustrated embodiment, a dome covering 514 is coupled around at least a portion of the second lumen 470. The dome covering 514 can shield the second lumen and the passage 510 from mucus. In some embodiments, the dome covering 514 forms a mushroom tip.
Some mushroom tip embodiments include holes in a tube with a domed surface covering the holes such that the holes are shielded from mucus or other substances. The holes can be round or any other suitable shape. In some embodiments, the holes are formed by a mesh weave, honeycomb shape, or knitted structure, which can provide more open surface area for air flow and more flexibility than some embodiments. The dome covering can connect to the distal end of the tubing. Several mushroom tips do not have struts.
The length of the dome covering 514 can vary among different embodiments. In some embodiments, the dome covering 514 is at least or equal to 2 mm long and less than or equal to 30 mm long; at least or equal to 3 mm long and less than or equal to 15 mm long; or at least or equal to 4 mm long and less than or equal to 8 mm long.
Several embodiments are similar to the embodiments described above except that the tips are fluidly coupled to a gas supply line to enable the tips to deliver oxygen or other gases through a passage in the body, such as a nasal passage. Several tip embodiments can be coupled to a gas sampling line or a gas supply line.
Tips can be attached to an adapter or can be integrally formed with an adapter. Some tips are attached directly to a sampling line rather than to an adapter.
In some embodiments, a tip is bonded or insert molded to catheter tubing that has extra holes to provide more air to the analyzer. The catheter tubing can have a malleable wire or ribbon located inside of the tubing to provide directionality for inserting the assembly into the nose and/or to hold the assembly in the nose. In
Some embodiments are magnetic resonance imaging (“MRI”) compatible. Thus, the embodiments present no additional risk to the patient and will not affect image quality. For example, in some embodiments, the wire 608 is titanium or another nonmagnetic metal. Some formable embodiments use stainless steel with a low reaction to magnetic fields.
Anchors can help more precisely place a tube in a portion of a patient's body (e.g., nasal passage). Anchors can lock and/or snuggly attach to catheters and/or adapters to assist with repeatedly placing and/or positioning catheters and/or adapters. Anchors can also prevent catheters and/or adapters from migrating too far into a portion of a patient's body.
Anchors 700 can have a tapered portion 704, a neck 708, a stabilizer 712, a slit 716, and an inner channel 720. The tapered portion 704 is configured to enable the anchor 700 to slide into a hole in a mask (as illustrated previously, e.g., holes 126 of mask 125 as shown in
In some embodiments, the anchor 700 easily slides on a catheter. When the anchor 700 (i.e., stop) is pushed into a hole in the mask, the slit 716 is closed and the anchor 700 is locked against (i.e., immobilized relative to) the catheter.
The tube 800 can be coupled to any of the tips and/or adapters described herein. In some embodiments, the tube 800 is used with the devices illustrated in
The following medical information is provided to explain the surprising nature of some of the above embodiments. This information applies to some embodiments, but may not apply to other embodiments. This information does not limit the scope of the inventions described herein.
Many airway detection systems are limited to use in shallow portions of nasal passages. While many embodiments described herein can be used in shallow portions of nasal passages, many embodiments can be used much deeper inside nasal passages than conventional airway detection systems. Increased depth can improve the accuracy and reliability of airway detection (e.g., as determined by waveform Capnography). Some embodiments enable nasopharynx sampling, which can result in reliably reproducible clinical data.
Placement of the sampling tube can be critical to patient safety and sampling accuracy.
The distance from nasal tip to choanae is approximately 4.85 cm in infants, 5.72 cm in children 2 to 6 years old, 7.3 cm in children 8 to 13 years old, and 7.59 cm in adults. The distance from nasal tip to posterior nasopharynx is approximately 5.94 cm in infants, 7.22 cm in children 2 to 6 years old, 8.78 cm in children 8 to 13 years old, and 9.91 cm in adults. Dimensions related to superior choanae also vary between infants, children, and adults. Monitoring exhaled breath in the choanal space or opening to the nasophyarynx can result in superior ETCO2 readings (i.e., the level of carbon dioxide released at the end of expiration).
Several method or use embodiments include monitoring exhaled air in the choanal space or opening to the nasophyarynx. The insertion depth can depend, at least in part, on the age and/or anatomy of the patient. Insertion depth can be particularly important for optimum detection in the choanal space and/or posterior nasopharynx. Insertion depth can also be important for the safety of the patient.
Some methods include placing a catheter deeper in an airway depending on the amount of gas flow (e.g., the higher the oxygen flow, the deeper the insertion). This disregard of the anatomy of patients in different patient groups could lead to increased injury, increased airway irritation (causing coughing, gagging, and/or bronchospasms) and even a life threatening situation called laryngeal spasm. A catheter that is placed too deeply in the nasopharynx and/or into the oral pharynx can lead to this life threatening situation. A laryngeal spasm (the spasm of the vocal cords causes partial or full closure of the vocal cords, allowing less gas exchange or zero gas exchange), can be a life threatening situation. Infants', children's, adolescents' and adults' airways can all be affected by irritations in the airway, which can trigger this spasm and cause undue harm.
Many catheter embodiments help to overcome this limitation. The catheters can have markings and can be secured to a mask or cannula to determine the average distance to the nasochoanal or posterior nasopharynx in different age groups allowing the medical professional to know where in the airway the device is approximately located. This method can optimize performance and safety of detection systems.
Artificial airway devices (such as nasopharyngeal airways and oropharyngeal airways) can be deeply placed devices (e.g., much deeper than some adapters). Catheters without markings could inadvertently be placed too deeply. Deeply placed devices should generally only be used with deeply sedated patients and patients who are obtunded, because placement of airway devices at this level can more readily irritate and cause life threatening spasms if the patient's natural airway reflexes are not diminished with sufficient sedation. Placing a device too deeply in the airway on a less sedated patient would increase the risk of a laryngeal spasm and airway complications. Several embodiments provide protection against this natural airway response. Some methods include placing a catheter no deeper than the nasopharynx and placing the catheter in the choanal space and/or posterior nasopharynx.
The small, sleek design of some embodiments and the smooth tip with protected holes of some embodiments combined with the formability of some embodiments can minimize tissue trauma. Airway devices placed deeply often are not tolerated by fully awake patients and can lead to gagging and coughing. In some cases, devices are not placed deeply unless the patient is sedated and cannot maintain her own breathing.
Flexible yet formable catheters (e.g., with a malleable wire or ribbon in a catheter wall) can provide the ability to direct the catheter into a precise location and/or enable repeated accurate sampling. In several embodiments, the precise location within the nasal passageway includes placement in the nasal choanal space, the posterior nasopharynx region, and/or the nasopharynx. This ability to direct the catheter also prevents blind insertion of a catheter into the nasal turbinates which are a series of three thin bone structures located superiorly in each nasal cavity. The turbinates are covered by spongy, mucous membranes and by delicate mucosal cells needed to humidify and filter the air we breathe. Damage to these delicate cells can lead to increased bleeding and possibly post-procedural sinusitis (especially in patients who are on anticoagulant therapy or are immunosuppressed).
The natural mucous layer or covering of these turbinates can easily occlude or clog an open tube as it is pushed through the nose. This can be more likely if the patient has allergies or any increased sinus drainage. A tube that is too flexible will simply bend back on itself and occlude when the medical professional pushes it through the nose. The tube can easily become lodged in between these turbinates and cause injury as well as show a false apnea reading or diminished ETCO2. At this point, the medical professional would have to remove the tube and start over, which could create the same potential problem. The ability to direct the catheter can alleviate this problem. The formability of the tube itself can allow the medical professional to direct the tube and even pre-form the tube to the natural curvature of the nare prior to insertion. The formable tube can follow the perpendicular plate of the palatine bone to the choanae more easily and with decreased trauma.
The formability of the adapter can also allow the medical professional to shape the tube for easier insertion into an oral or nasal airway. Placing a flexible tube that has holes in an artificial airway can cause the detection holes to lay against the internal surface of the airways and not detect ETCO2 correctly. A formable tube that is pre-shaped in approximately the same design as these airways will have less collection holes occluded, which can enable improved detection of ETCO2.
Infants are sometimes obligate nasal breathers that prefer to breathe through their nose. The adapter and/or tip can be extremely helpful in a more accurate detection of ETCO2. The choanae is much closer to the lungs and away from the dilution of the standard nasal cannulas, which can lead to more accurate accounting of ETCO2 and cause less trauma.
Placing a nasal cannula for ETCO2 detection on a child's small face and then placing a mask on top of the cannula is extremely uncomfortable and cumbersome. It can also lead to dilution problems. Infants often require more accurate monitoring of ETCO2 due to their sensitivity to hypoxia and apnea. A premature infant and/or child cannot tolerate hypoxia and abnormal ETCO2 as well as adults. The formability can allow for safer and less traumatic passing of a catheter into the choanae and can allow for more accurate ETCO2 monitoring. Many embodiments provide less diluted sampling and/or sampling closer to the lungs.
Capnography involves the monitoring of the concentration or partial pressure of carbon dioxide. Capnography results can be displayed as a carbon dioxide graph. Clogged sensing holes can jeopardize the accuracy of capnography and lead to false medical conclusions. Medical professionals often have to guess whether capnography results are accurate or are based on clogged tubes. Partially shielded sensing holes can improve the reliability and accuracy of capnography for at least one of several reasons. The sampling tube can be placed deeper inside a nasal passage than would be possible with an unshielded system. While pushing an unshielded system deep within the nasal passage would drive mucus into the sample tube and cause tissue trauma, pushing a shielded system significantly increases the likelihood of unobstructed sampling holes and a domed tip can reduce tissue trauma. Moreover, a deeper sampling location can result in less carbon dioxide dilution that is common with shallow sampling locations.
Capnography can be performed with various monitoring devices including capnographs and capnometers. Many different types of gas analyzers can be used with the embodiments disclosed herein.
Achieving steady, accurate capnography waveforms is difficult with traditional systems. Medical professionals often spend time repositioning the sampling tube to improve waveforms. (In some cases, shallow breathing as frequently seen with moderate to deep sedation produces lower tidal volumes, which can make traditional nasal cannula styles and/or methods unable to detect ETCO2 accurately.) The ability to more accurately monitor ventilation provides important data and safer patient care.
Experiments are performed to evaluate the performance of the nasal carbon dioxide detectors described herein, as compared to the nasal device described in U.S. Patent Application Publication 2011/0009763, which was assigned to Oridion Medical 1987 Ltd. The two types of nasal capnography devices are connected to conventional carbon dioxide monitors and the concentration and/or partial pressure of exhaled carbon dioxide is evaluated in a subject (e.g., a laboratory animal, such as a pig or a human, for example a volunteer test subject or a patient). The levels of carbon dioxide sampled by the devices are then compared via Capnography and/or via the waveforms on a capnograph. It is expected that the nasal carbon dioxide detection devices disclosed herein (e.g., one or more of the embodiments depicted in
The first device is constructed from conventional, flexible, medical-grade tubing having a blunt-open end and further comprising a plurality of holes within the blunt open-end. (See FIG. 2 of U.S. Patent Application Publication 2011/0009763, herein expressly incorporated by reference in its entirety). This device has a plurality of holes that are oriented radially outward relative to a central axis of the second device. The plurality of holes are located near the distal end of the device. The blunt end of the device, which comprises the plurality of holes, is inserted into the subject's nasal passage way.
The second device is constructed as set forth herein with reference to
Ideally, the two devices are analyzed on the same patient successively. That is, the first device is placed into the patient and the concentration and/or partial pressure of exhaled carbon dioxide is evaluated in the subject with the carbon dioxide monitor, and preferably, the waveforms generated by the exhaled carbon dioxide are recorded. The first device is removed, and then the second device is placed into the subject. The second device is then used to evaluate the concentration and/or partial pressure of exhaled carbon dioxide in the subject with the carbon dioxide monitor, and the waveforms generated by the exhaled carbon dioxide are recorded, as before. The second device is then removed. The two devices can be compared via comparing waveforms according to methods of Capnography. A standard normal waveform comparison is conducted for both devices.
It will be seen that the shielded devices (the second device), e.g., the devices illustrated in
Some device comparisons use multiple devices and include a device constructed according to
In some cases, patients do not have so much mucous that clogging is a substantial problem, but in many cases, patients have sufficient mucous to make clogging a challenge from some devices. It is contemplated that the second device will be found to be less prone to clogging than the first device.
In some device comparisons, the performance of each device is measured by the carbon dioxide detection accuracy, patient comfort, and/or patient safety. It is expected that some comparisons will show several of the embodiments disclosed herein enable more accurate carbon dioxide detection, less patient discomfort, and superior patient safety than several prior art devices.
Many of the embodiments disclosed herein are special because of their ability to monitor deeper and more accurately than some alternative devices. It will be shown that some of the embodiments disclosed herein enable deeper, safer, more stable, more reliable, and/or more accurate carbon dioxide monitoring than some devices currently approved by the U.S. Food and Drug Administration. Some of the embodiments are adaptable for use with any nasal cannula, any mask, and any artificial airway device.
Several embodiments are formable to assist in insertion (e.g., not blindly inserted) and to allow the embodiments to be more directable, which can allow practitioners to be able to push the embodiments passed enlarged adenoids for detection in children and other patients.
In some embodiments, small, sleek designs make insertion safe and trauma-free to delicate nasal mucous due to a soft, rounded and/or dome shaped tip. The specially designed tips can allow for a protective covering from nasal material if necessary to sample CO2 more accurately.
Some embodiments have markings to allow practitioners to know where in the nasal anatomy they are actually sampling. The markings can make the product safer (even in the absence of the other improvements highlighted herein).
In some cases, there is an actual correlation or marking on the catheter that tells the practitioner where they have inserted the catheter. A catheter placed too deeply in the nasopharynx can result in complications.
Some embodiments include and/or enable sampling at the opening of the nasopharynx and at the posterior nasopharynx. Some embodiments include and/or enable sampling at a specific region (e.g., target region) such as at the opening or just inside the nasopharynx. Some embodiments include ETCO2 detection.
The pharynx is divided into 3 parts: the nasopharynx, oropharynx, and the hypopharynx. The nasopharynx extends from the base of the skull to the upper surface of the soft palate. Its cavity differs from the oropharynx and hypopharynx due to its patency (i.e., openness). The nasochoanal space is the opening to the nasopharynx, and frequently is described as a funnel shaped space. The choanal space creates a wide opening to a more narrow structure, the nasopharynx. The choana, which is made up of boney structures of the airway, is not collapsible, remains patent, and is ideal (according to some embodiments) for monitoring due to its fixed, rigid anatomical make up. Sampling in the nasochoanal space and/or in the nasopharynx can lead to more accurate detection of ETCO2 regardless of the amount of oxygen supplied due to its depth in the airway. Current nasal cannuals for ETCO2 sampling typically sample at the edge of the nare where oxygen is delivered and also can sample at a point furthest from the trachea and/or lungs, which can add to the dilution factor. Several embodiments disclosed herein can sample in ideal (e.g., the choanal region) and less than ideal locations, based on medical need, medical training, and preferences of the medical practitioner.
Sampling in the shallow nare and upper nasal airways (i.e., turbinates) can result in more diluted and/or less accurate detection and/or sampling of ETCO2. When a patient receives supplemental oxygen via a nasal cannula or a mask, air flow patterns (e.g., vortex patterns) can develop with in the upper nasal passageway. This can lead to increase dilution of the ETCO2 gas that is naturally being expired by the patient. A catheter placed deeply and intentionally into the nasochaonal space (also referred to as the choanal region) to the nasopharynx can improve the detection of ETCO2 due to its proximity in the airway to the trachea/lungs and distance away from the oxygen delivery source. Sampling in this location can result in a less diluted sample and therefore a more accurate detection of ETCO2.
The nasopharynx, unlike the choanae, is made up of soft tissue and is collapsible as is frequently seen in conditions such as obstructed sleep apnea and seen with enlarged adenoids (a collection of lymphoid tissue located in the roof of the nasopharynx). Adenoid hypertrophy is usually only present in young children. This tissue is usually nonexistent in children 5-6 years old and beyond. Even when adenoid hypertrophy is present, the soft tissue is distensible and devices such as nasogastric tubes and endoscopes can be passed safely. In several embodiments, the adapter can also be passed safely to monitor ETCO2 in this patient population.
In several embodiments, adapter devices described herein can overcome some of these limitations of monitoring ETCO2 in a narrow or partial collapsed nasopharynx due to the formability, directability, and/or marking of the adapter assemblies. Some adapter assemblies include markings based on and/or tailored to specific age groups to allow medical professionals to know where the catheter is located in the airway.
The formability of the catheter can give the adapter stability and make it easier to safely and precisely direct or advance the adapter into the shallow nare, through the choanal space, and into the nasopharynx, which may or may not be narrowed. A stable, formable catheter can be easier to advance in the nasopharynx to detect ETCO2 without kinking or causing trauma. A more stable catheter can be pushed past an enlarged adenoid to monitor ETCO2 in various age groups. The catheter's specially designed tip can make the catheter more comfortable and can facilitate sampling and/or detecting ETCO2 in narrow areas of the airway due to formability, sleek design, and the collection of protected sampling pores.
As used herein, the terms “comprise,” “comprises,” “comprising,” “having,” “including,” “includes,” or any variation thereof, are intended to reference a non-exclusive inclusion, such that a process, method, article, system, composition or apparatus that comprises a list of elements does not include only those elements recited, but may also include other elements not expressly listed or inherent to such process, method, article, system, composition or apparatus. Other combinations and/or modifications of the above-described structures, arrangements, applications, proportions, elements, materials or components used in the practice of the present invention, in addition to those not specifically recited, may be varied or otherwise particularly adapted to specific environments, manufacturing specifications, design parameters or other operating requirements without departing from the general principles of the same.
In the foregoing specification, the invention has been described with reference to specific embodiments. Various modifications and changes may be made, however, without departing from the scope of the various embodiments of the present invention, as set forth in the claims. The specification and Figures are illustrative, rather than restrictive, and modifications are intended to be included within the scope of any of the various embodiments of the present invention described herein. Accordingly, the scope of the invention should be determined by the claims and their legal equivalents rather than by merely the examples described.
For example, the steps recited in any method or process claims may be executed in any order and are not limited to the specific order presented in the claims. Additionally, the components and/or elements recited in any apparatus or system claims may be assembled or otherwise operationally configured in a variety of permutations and are accordingly not limited to the specific configuration recited in the claims.
Benefits, other advantages and solutions to problems have been described above with regard to particular embodiments; however, any benefit, advantage, solution to problem or any element that may cause any particular benefit, advantage or solution to occur or to become more pronounced are not to be construed as critical, required or essential features or components of any or all the claims.
This application is a continuation-in-part of and claims the benefit of priority to U.S. patent application Ser. No. 13/360,390, entitled Method and Device for Monitoring Carbon Dioxide, filed on Jan. 27, 2012, which claims the benefit of priority to U.S. Provisional Patent Application No. 61/436,716, entitled Method and Device for Monitoring Carbon Dioxide, filed on Jan. 27, 2011 and, which claims the benefit of priority to U.S. Provisional Patent Application No. 61/565,950, entitled Method and Device for Monitoring Carbon Dioxide, filed on Dec. 1, 2011. All of the aforementioned provisional applications and patent application are hereby expressly incorporated by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| 61436716 | Jan 2011 | US | |
| 61565950 | Dec 2011 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13360390 | Jan 2012 | US |
| Child | 13954862 | US |
