DEVICE TO SECURE AIRWAY DURING EMERGENCY CARE

FIELD

A device, kit and method for securing an airway during emergency care. Other embodiments are also described herein.

BACKGROUND

Airway management of an individual in an emergent medical event is the most critical determinant of the survival and long term outcomes. Studies have shown that in pre-hospital care settings, intubation in the field by emergency medical technicians (EMT) may delay the time to cardiopulmonary resuscitation and chest compression, and does not improve overall outcomes in comparison to using bag-mask ventilation (BMV). BMV remains the current standard for airway and ventilation for unconscious individuals, particularly infants and children, in pre-hospital care settings.

While BMV is the cornerstone of basic airway management, many problems have been reported with BMV use in children. First, BMV requires the mask to be firmly pressed on the patient's face, thus inadequate pressure or inappropriate size of the mask may cause air leak making the ventilation inefficient. Maintaining a good airtight seal for a prolonged period of time could be challenging. Pressing the mask requires one or both hands of the EMT and thereby reduces the availability of personnel in pre-hospital care settings where hands may be limited. Furthermore, BMV may not be practical in patients with facial trauma, unstable cervical spine or a potential unstable airway. Also, when a patient vomits, inexperienced users of BMV may not recognize it immediately resulting in aspiration, which can lead to pneumonia and ARDS.

Many supraglottic airway devices have been designed to improve the problems associated with BMV. These devices, such as the laryngeal mask, require advanced skills and thus are commonly used by anesthesiologists instead of by EMT in pre-hospital care settings. One representative airway device, which is designed to provide secure airway and prevent aspiration, includes two balloons: one in the esophagus, one in the oropharynx. Due to the positioning of the balloons, however, this device typically requires advanced training and many problems have been reported with its use. Representative problems can include nerve plexus damage, venous thrombosis, compromised carotid flow, and post-extubation swelling. Another type of airway device commonly used is known as a cuffed oral airway device. Use of the cuffed oral airway device, however, is still associated with oropharyngeal compression, post-extubation swelling, and cannot be used in patients who are unconscious and apneic.

SUMMARY

The airway device disclosed herein provides an improvement over typical airway devices in that it is useful: 1) for pre-hospital care of infants, children and adults by EMT; and 2) as a rescue airway until endotracheal intubation can be performed by more skilled personnel (e.g. in a hospital setting). In this aspect, the airway device is configured to deliver pumped air to the trachea without endotracheal intubation. Representatively, in one embodiment, the airway device includes a hollow tube dimensioned for insertion through the patient's mouth to the esophagus. An oral cavity balloon dimensioned to block the oral cavity is positioned at one end of the tube and an esophageal balloon dimensioned to block the esophagus is positioned at another, closed, end of the tube. Apertures are further provided in a side of the tube that is aligned with the oropharynx. In this aspect, when air is pumped into the one end of the tube, it passes through the tube and out the apertures to the oropharynx. A nose block may further be provided such that the only way for air pumped into the tube to go is out the apertures and to the trachea. In this aspect, the airway device allows for air to be pumped directly into the trachea. Furthermore, the esophageal balloon prevents reflux of gastric content from causing aspiration. In addition, positioning of the oral cavity balloon in oral cavity, instead of the oropharynx, avoids compression of vital structures (nerve plexus, venous sinuses and carotid arteries).

BRIEF DESCRIPTION OF THE DRAWINGS

The following illustration is by way of example and not by way of limitation in the figures of the accompanying drawings in which like references indicate like elements. It should be noted that references to “an” or “one” embodiment in this disclosure are not necessarily to the same embodiment, and such references mean at least one.

FIG. 1 illustrates a cross-sectional side view of one embodiment of an airway management device.

FIG. 2A illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 1.

FIG. 2B illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 1.

FIG. 3A illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 1.

FIG. 3B illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 1.

FIG. 4 illustrates a cross-sectional side view of another embodiment of an airway management device.

FIG. 5A illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 4.

FIG. 5B illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 4.

FIG. 6A illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 4.

FIG. 6B illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 4.

FIG. 7A illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 4.

FIG. 7B illustrates a cross-sectional side view of one embodiment of the airway management device of FIG. 4.

FIG. 8 is a block diagram illustrating one embodiment of an airway management process.

DETAILED DESCRIPTION

In this section we shall explain several preferred embodiments of this invention with reference to the appended drawings. Whenever the shapes, relative positions and other aspects of the parts described in the embodiments are not clearly defined, the scope of the invention is not limited only to the parts shown, which are meant merely for the purpose of illustration. Also, while numerous details are set forth, it is understood that some embodiments of the invention may be practiced without these details. In other instances, well-known structures and techniques have not been shown in detail so as not to obscure the understanding of this description.

FIG. 1 illustrates a cross-sectional side view of one embodiment of an airway management device positioned within an airway of a user. In one embodiment, airway management device 100 may be positioned within an airway of a patient 102, which could be a mammal of any age and size. Representatively, in one embodiment, airway management device 100 is dimensioned for management of an airway of a human within any of the following age ranges: newborn (<30 days old), infant (1 month to 11 months), toddler (1-3 years), young child (4-10 years), older child (11-14 years) or adolescents and adults (>15 years). In other embodiments, airway management device 100 may be dimensioned for use in an animal of any size and shape (e.g. a dog, a cat, a pig, a horse, a cow, etc.). In the illustrated embodiment, patient 102 is a human.

As previously discussed, often times when the patient becomes unconscious, it is necessary for a care provider to manage the patient's breathing by manually introducing air into the lungs. Typically, in a healthy individual, air passage to the lungs occurs when the individual breathes air in through nose 124 or mouth 128. In the case of the mouth, air passes from mouth 128, through oral cavity 116 and into the oropharynx 118, which is the oral part of the pharynx extending from the uvula to the hyoid bone. Air from nose 124 passes through nasal cavity 130 and also into oropharynx 118. From oropharynx 118, the pathway splits into the trachea 122, which extends to the lungs, and the esophagus 120, which extends to the stomach. Thus, in order to introduce air to the lungs, air management device 100 is dimensioned to create a substantially sealed air pathway from mouth 128 to trachea 122. Representatively, air management device 100 is dimensioned to deliver air to oropharynx 118 while blocking the esophagus 120 and air exits from nose 124 and mouth 128 such that the only way for pumped air to go is to the trachea 122.

To create such a sealed pathway, in one embodiment, airway management device 100 includes tubular member 104, which is dimensioned to extend through mouth 128 to esophagus 108. An end of tubular member 104 extending from mouth 128 is open to allow for the introduction of air and the other end is sealed to prevent air from exiting out the end and into esophagus 120. Apertures 120 are formed within a portion of tubular member 104 near the sealed end and within oropharynx 118 such that air introduced into the open end exits through apertures 120 toward trachea 122. Airway management device 100 may further include an inflatable oral cavity balloon 106, which can be inflated within the oral cavity 116 to help position tubular member 104 within the air pathway of patient 102 and prevent air from exiting mouth 128 during a ventilation procedure. In addition, airway management device 100 includes an inflatable esophageal balloon 108 positioned near the sealed end of tubular member 104, which can be inflated within or at an entrance to esophagus 120 to prevent air from entering esophagus 120. In addition to preventing air entry, inflatable esophageal balloon 108 may be dimensioned to prevent reflux of gastric content from esophagus 120 without putting excessive pressure on the esophageal wall.

Airway management device 100 may further include protrusion 110 which extends from a middle portion of tubular member 104 in a direction of tongue 130. Protrusion may be dimensioned to serve as a tongue holder which holds tongue 130 in place during inflation of oral cavity balloon 106 and prevents tongue 130 from posterior displacement thus blocking the air pathway to trachea 122. Air management device 100 may also include bite block 114. Bite block 114 may be positioned along a portion of tubular member 104 positioned near the teeth so that if patient 102 bites down during the ventilation procedure, the force from the bite does not collapse the tube thus obstruct air passage through the airway management device 100. Bite block 114 may further serve as a guide to help properly position airway management device 100 within the patient 102.

In some embodiments, a nose block 126 may further be provided. Nose block 126 may be any type of nose blocking device such as a nose clip or other mechanism capable of sealing nose 124 that can occlude the nostrils and prevent air exits through nose 124. It is further contemplated that in some embodiments, a pulse oximeter sensor or other similar sensing device may be integrated with, or placed near, the nose block 124 such that the oxygen saturation or other physiologic parameters of the patient can be monitored during the ventilation procedure.

Each of the aspects of airway management device 100 will now be described in further detail in reference to FIG. 2A, FIG. 2B, FIG. 3A and FIG. 3B. Referring to FIG. 2A and FIG. 2B, FIG. 2A illustrates a cross-sectional side view of airway management device 100 in a deflated configuration and FIG. 2B illustrates a cross-sectional side view of airway management device 100 in an inflated configuration. FIG. 3A illustrates a cross-sectional top view of airway management device 100 in a deflated configuration and FIG. 3B illustrates a cross-sectional top view of airway management device 100 in an inflated configuration.

Returning to FIG. 2A-2B, from this view it can be seen that tubular member 104 is a hollow tube having a proximal portion 202, a middle portion 206 and a distal portion 204. During use, proximal portion 202 is positioned within the oral cavity while distal portion 204 is positioned into the esophagus of the patient. Middle portion 206 of tubular member 104 may form a bend such that tubular member 104 substantially conforms to the curvature of the air pathway of the patient and can be advanced through oral cavity 116 to esophagus 120. In some embodiments, open end 210 of tubular member 104 may have the dimensions of a universal connector used in endotracheal tubes for connection with an Ambu-bag or ventilator. In some embodiments, tubular member 104 may be made of any semi-rigid material such as polyethylene or a clear polyvinyl chloride (PVC) suitable for insertion along an air passageway of a patient. In addition, in some embodiments, the diameter of tubular member 104 may taper toward sealed end 208 and the material used in the esophageal portion (i.e. distal portion 204) may be less rigid than other portions of tubular member 104 (e.g. middle portion 206 and/or proximal portion 202) to avoid esophageal injury.

Inflatable oral cavity balloon 106 may be mounted to proximal portion 202 of tubular member 104 so that when tubular member 104 is in place, oral cavity balloon 106 is positioned within oral cavity 116 as illustrated in FIG. 1. In one embodiment, inflatable oral cavity balloon 106 may be positioned at a region of tubular member 104 and dimensioned such that it only occludes oral cavity 116 and does not occlude nasal cavity 130. In other words, oral cavity balloon 106 may be confined to the oral cavity 116 and does not extend to other regions such as the oropharynx 118, or other regions adjacent middle portion 206. Rather, oral cavity balloon 106 is positioned between bite block 114, and in some cases contacting bite block 114, and the bend portion of middle portion 206. Inflatable oral cavity balloon 106 may be substantially symmetric in the inflated configuration as shown. In other embodiments, oral cavity balloon 106 may be substantially asymmetric in the inflated configuration. Representatively, the distal end of oral cavity balloon 106 may have a larger diameter than the proximal end. This type of structure may help to compress and push the tongue forward such that oral cavity balloon 106 can also serve as a tongue holder. Alternatively, the distal end of oral cavity balloon 106 may have a smaller diameter than the proximal end to facilitate blocking of the oral cavity.

Oral cavity balloon 106 may be a substantially compliant balloon made of materials including, but not limited to, latex, polyurethane, nylon elastomers and other thermoplastic elastomers. In this aspect, oral cavity balloon 106 can be inflated until it fills the oral cavity and provides a seal in order to prevent air leak through the mouth. Oral cavity balloon 106 may be inflated and/or deflated by connecting a syringe (not shown) to inflation tube 214 which extends along tubular member 104 to oral cavity balloon 106. Injecting air via the syringe will in turn deliver air to oral cavity balloon 106 causing oral cavity balloon 106 to inflate. Oral cavity balloon 106 may be deflated by withdrawing air through inflation tube 214 using the syringe. In some embodiments, inflation tube 214 may extend through the lumen of tubular member 104 and through the wall to oral cavity balloon 106. Alternatively, inflation tube 214 may extend along the outside of tubular member 104.

In some embodiments, esophageal balloon 108 may also be connected to inflation tube 214. In this aspect, oral cavity balloon 104 and esophageal balloon 108 may be inflated or deflated at the same time or in sequence (by varying the resistance of balloons to allow esophageal balloon to fill up first then the oral cavity balloon). In other embodiments where independent inflation/deflation of esophageal balloon 108 is desired, a separate inflation tube may be connected to esophageal balloon 108. As previously discussed, esophageal balloon 108 is used to block the opening to esophagus 120 as illustrated in FIG. 1. Esophageal balloon 108 may therefore be mounted to distal portion 204 of tubular member 204, near sealed end 208. Esophageal balloon 108 may be less compliant than oral cavity balloon 104 such that it can be inflated to a predetermined maximum size suitable for blocking an opening of the esophagus (e.g. to block acid reflux from the stomach) without putting excessive pressure on the esophageal wall. Representatively, in one embodiment, esophageal balloon 108 may be made of a polyethylene or other low-compliance polymer and have a maximum diameter which is substantially equal to that of the esophageal opening.

To facilitate positioning of oral cavity balloon 104 and esophageal balloon 108 at the desired region within the patient, tubular member 104 may have a length (and bend as previously discussed) such that when tubular member 104 is positioned within the patient, oral cavity balloon 104 is positioned within oral cavity 116 and esophageal balloon 108 is positioned within the superior portion of esophagus 120. Representatively, tubular member 104 may have any length and oral cavity balloon 104 and esophageal balloon 108 any dimension/shape suitable for positioning of airway management device 100 within an airway path as described above for patients within any of the following age ranges: newborn (<30 days old), infant (1 month to 11 months), toddler (1-3 years), young child (4-10 years), older child (11-14 years) or adolescents and adults (>15 years). The dimensions and shape of tubular member 104, oral cavity balloon 104 and esophageal balloon 108 may also be suitable for use of the airway management device 100 within a patient that is an animal (e.g. a horse, a cow, a pig, a dog, a cat, etc).

Protrusion 110 may extend from tubular member 104, near or within proximal portion 202 so that it is aligned with the tongue when air maintenance device 100 is positioned within the oral cavity. In some embodiments, protrusion 110 may have a substantially triangular profile with the distal portion being the base of the triangle and extending further from tubular member 104 farther than the proximal portion. In this aspect, the wider portion of protrusion 110 pushes the back portion of the tongue away from apertures 112 formed within proximal portion 206 so that it does not block apertures 112, or other air pathways.

Apertures 112 are formed within the middle portion 206 of tubular member 104 so that they are aligned within the oropharynx 118 (see FIG. 1) of the patient when device 100 is in place. Although a plurality of apertures 112 are shown, it is contemplated that any number and diameter of apertures 112 suitable for delivering outputting air to the trachea of the patient may be formed through tubular member 104. Representatively, in some embodiments, there may be only one of apertures 112 (e.g. one large aperture) while in another embodiment there is more than one of apertures 112 (e.g. a plurality of smaller apertures). In this aspect, when air is pumped through tubular member 104, air will flow through apertures 112 to the oropharynx. Since the exits to the mouth, nose and esophagus are sealed via oral cavity balloon 106, nose block 126 and esophageal balloon 108, respectively, the pumped air will be forced to the trachea. In addition, any expired air from the trachea can exit the trachea through tubular member 104.

In some embodiments, nose block 126 may be attached to airway management device 100 while in others nose block 126 may be separate from airway management device 100. Representatively, nose block 126 may be attached to airway management device 100 by a chord 212 attached to the proximal portion 202 of tubular member 104 so that nose block 126 is near the patient's nose when airway management device 100 is inserted within the patient's mouth. Once airway management device is in the desired position, nose block 126 can be positioned around the patient's nose to block air from exiting the nose. As previously discussed, nose block 126 may be any type of nose clip or other mechanism capable of restricting air passage through the patient's nose (e.g. a nose plug).

FIG. 3A and FIG. 3B illustrate top views of airway management device 100 in the deflated and inflated configurations, respectively. From this view, it can be seen that protrusion 110 may have a width dimension greater than that of tubular member 104 such that it extends beyond the sides of tubular member 104. In some embodiments, protrusion 110 may have a width dimension substantially similar to that of the patient's tongue width such that it can hold a substantial portion of the tongue in the desired position without the sides of the tongue curling up. It can further be seen from this view that in some embodiments, apertures 112 can extend around a substantial portion of the circumference of tubular member 104. For example, apertures 112 may be formed within both the sides of tubular member 104 near or facing the trachea and the top of tubular member 104.

One representative way of using airway management device 100 will now be described. For example, in one embodiment, airway management device 100 having the appropriate dimensions for the patient is selected by the care provider (e.g. EMT). With both the oral cavity balloon 106 and esophageal balloon 108 deflated, tubular member 104 is placed within the patient's mouth and pointed posterior to prevent the tube from entering into the trachea. This part can be performed by properly placing the patient's head and opening the mouth manually without the use of a laryngoscope. Tubular member 104 is then advanced until protrusion 110 is aligned with the base of the tongue. Nose block 126 may then be placed on the nose to block the nasal airway. A syringe (not shown) is connected to the inflation tube 214. Using the syringe, air is then pumped through inflation tube 214 and into oral cavity balloon 106 and esophageal balloon 108 until the oral cavity balloon 106 fills up and occludes the oral cavity so that air cannot exit. An Ambu-bag, or other hand-held device capable of providing positive pressure ventilation, is attached to the open end 210 universal connector of tubular member 104. The user then ventilates the patient by compressing the bag to pump air through tubular member 104 and into the trachea via apertures 112. Successful placement of airway management device 100 and adequate ventilation can be assessed by observing chest rise of the patient and auscultation of air movement using a stethoscope.

FIG. 4 illustrates a cross-sectional side view of another embodiment of an airway management device positioned within an airway of a user. In one embodiment, airway management device 400 may be positioned within an airway of a patient 402, which could be a mammal of any age and size as previously discussed in reference to FIG. 1. Airway management device 400 may be substantially similar to airway management device 100 described in reference to FIG. 1 except that in this embodiment, device 400 includes an oral airway tube 404 and an esophageal tube 403 positioned concentrically inward of the oral airway tube 404. Oral airway tube 404 is dimensioned to pass from the mouth 428, through oral cavity 416 and to the base of the tongue 430. An inflatable oral cavity balloon 406 is attached to oral airway tube 404 so that in the inflated configuration, oral cavity balloon 406 can be used to block air exit from mouth 428. Esophageal tube 403 is dimensioned to extend through oral airway tube 404, from the mouth 428 to the esophagus 420. An inflatable esophageal balloon 408 is attached to the end of esophageal tube 403 near esophagus 420 and aperture 412 is formed within the portion of esophageal tube 403 positioned within the oropharynx 418. Similar to airway management device 100, the patient's oral airway and nasal airway may be blocked using oral cavity balloon 416 and nose block 426, respectively, and the pathway to esophagus 420 blocked using esophageal tube 403 such that the only way for air pumped through esophageal tube 403 to go is out aperture 412 to trachea 422.

Airway management device 400 may also include bite block 414. Bite block 414 may be positioned along a portion of oral airway tube 404 positioned near the users teeth so that if patient 402 bites down during the ventilation procedure, the force from the bite does not obstruct operation of airway management device 400. Bite block 414 may further serve as a guide to help properly position airway management device 400 within the patient 402.

In some embodiments, although not illustrated, an optional tongue holder may further be provided to hold tongue 430 in place during inflation of oral cavity balloon 406.

Each of the aspects of airway management device 400 will now be described in further detail in reference to FIG. 5A, FIG. 5B, FIG. 6A, FIG. 6B, FIG. 7A and FIG. 7B. FIG. 5A and FIG. 5B illustrate cross-sectional side views of one embodiment of the oral airway tube of FIG. 4 in a deflated configuration and an inflated configuration, respectively. In one embodiment, oral airway tube 404 includes a proximal portion 502 terminating at a proximal end 540, and a distal portion 504 terminating at a distal end 542. When airway management device 400 is positioned within the airway of the patient, proximal end 504 may be near mouth 428, and in some cases extend from mouth 428, while distal end 542 is positioned near the base of the tongue. Each of the proximal end 540 and the distal end 542 are open and oral airway tube 404 may have a lumen large enough to allow for insertion of esophageal tube 403 therethrough. Proximal end 540 can also be dimensioned to accommodate a universal adaptor that can be connected to an ambu-bag or other ventilating device. In some embodiments, oral airway tube 504 may be a semi-rigid tube made of, for example, polyethylene.

Oral cavity balloon 406 may be attached to the proximal portion 402 of oral airway tube 404 and positioned within the oral cavity of the patient during use. Oral cavity balloon 406 may be a substantially compliant inflatable/deflatable balloon having an outer diameter sufficient to fill the oral cavity and provide a substantially complete seal in order to prevent air leak via the mouth. In some embodiments, oral cavity balloon 406 may be an asymmetrical balloon such that when it is inflated, the proximal end diameter is greater than that of the distal end, or the distal end diameter is greater than that of the proximal end. Oral cavity balloon 406 may be made of any compliant material such as latex, polyurethane, nylon elastomers and other thermoplastic elastomers. Bite block 414 may be attached to the proximal portion 502 of oral airway tube 404 such that it is aligned with the teeth of the patient when oral airway tube 404 is positioned within the patient's oral cavity.

Oral cavity balloon 406 may be inflated and/or deflated by connecting a syringe (not shown) to inflation tube 514 which extends along oral airway tube 404 to oral cavity balloon 406. Injecting air into the syringe will in turn deliver air to oral cavity balloon 406 causing oral cavity balloon 406 to inflate. Oral cavity balloon 406 may be deflated by withdrawing air through inflation tube 514 using the syringe. In some embodiments, inflation tube 514 may extend through the lumen of oral airway tube 404 and through the wall to oral cavity balloon 406. Alternatively, inflation tube 514 may extend along the outside of oral airway tube 404.

FIG. 6A and FIG. 6B illustrate cross-sectional side views of the esophageal tube of FIG. 4 in a deflated and an inflated configuration, respectively. Esophageal tube 403 includes a proximal portion 602 terminating at a proximal end 640, and a distal portion 604 terminating at a distal end 642. Esophageal tube 403 may further include a middle portion 606, between proximal portion 602 and distal portion 604, and having a bend so that esophageal tube 403 can conform to a shape of the air pathway of the patient. Esophageal tube 403 may have a length such that when airway management device 400 is positioned within the airway of the patient, proximal end 604 may be near mouth 428, and in some cases extend from mouth 428, while distal end 642 is positioned near, or within, the esophagus 420. Proximal end 640 may be a substantially open end and the distal end 642 may be a sealed end such that air pumped into esophageal tube 604 can only exit through aperture 412. Esophageal tube 403 may have an outer diameter smaller than the inner diameter of the inner diameter of the oral airway tube 504 such that it can be inserted within and through oral airway tube 404. In some embodiments, when esophageal tube 403 is inserted through oral airway tube 504, proximal end 640 may be dimensioned to extend from the proximal end 540 of oral airway tube 504 and accommodate a universal adaptor that can be connected to an ambu-bag or other ventilating device. In some embodiments, esophageal tube 403 may be made of a clear PVC, or other similar material.

In some embodiments, esophageal balloon 408 is connected to the distal portion 604 of esophageal tube 403. An inflation tube 614, separate from inflation tube 514, may extend from the proximal end 602 to the distal end 604 and connect to esophageal balloon 408 to allow for inflation and deflation of esophageal balloon 408. Inflation tube 614 may run along the inner lumen of esophageal tube 403 or outside of esophageal tube 403. As previously discussed, esophageal balloon 408 is used to block the opening to esophagus 420 as illustrated in FIG. 4. In some embodiments, esophageal balloon 408 may be less compliant than oral cavity balloon 404 such that it can be inflated to a predetermined maximum size suitable for blocking an opening of esophagus 420 (e.g. to block acid reflux from the stomach) without putting excessive pressure on the esophageal wall. Representatively, in one embodiment, esophageal balloon 408 may be made of a polyethylene or other low-compliance polymer and have a maximum diameter which is substantially equal to that of the esophageal opening.

Esophageal tube 403 may further include aperture 412 formed within distal portion 604. Aperture 412 may be a single opening or a plurality of openings formed through a portion of the wall of esophageal tube 403.

A stopper 620 may further be attached to the distal portion 602 of esophageal tube 403. Stopper 620 may be dimensioned to prevent proximal end 640 of esophageal tube 403 from being inserted through oral airway tube 404. In one embodiment, stopper 620 may be a ring shaped member which increases a diameter of oral airway tube 404. In this aspect, during an assembly operation, distal end 642 of esophageal tube 403 can be inserted through the proximal end 540 of oral airway tube 404 and pulled out the distal end 542 of oral airway tube 404 until stopper 620 reaches bite block 414 as illustrated in FIG. 7A and FIG. 7B.

FIG. 7A and FIG. 7B illustrate cross-sectional side views of the assembled airway management device 400. From this view, it can be seen that when esophageal tube 403 is inserted through oral airway tube 404, oral airway tube 404 may overlap esophageal tube 403 along its proximal portion 602 and middle portion 606 such that the proximal end 640 and distal portion 604 of esophageal tube 403 are exposed. In this aspect, aperture 412 is positioned between the distal end 542 of airway tube 404 and the distal end 642 of esophageal tube 403, and exposed to the oropharynx (see FIG. 4). Since all the airway paths other than the trachea 422 are blocked by oral cavity balloon 404, esophageal balloon 408 and nose block 426, air exiting aperture 412 to the oropharynx 418 passes to trachea 422 and to the lungs. It is noted that in some embodiments, nose block 426 is attached to oral airway tube 404 or esophageal tube 403 via chord 712 as illustrated, while in other embodiments, nose block 426 is separated from airway management device 400.

One representative way of using airway management device 400 will now be described. For example, in one embodiment, the airway management device 400 having the appropriate dimensions for the patient is selected by the care provider (e.g. EMT). Oral airway tube 404 and esophageal tube 403 may be inserted into the patients airway separated or as an assembled unit. For example, in one embodiment, oral airway tube 404 is first inserted into the patient's oral cavity followed by insertion of esophageal tube 403 through oral airway tube 404. Alternatively, esophageal tube 403 is inserted through oral airway tube 404 prior to positioning within the patient, and then the two together are inserted within the patient's mouth as a preassembled unit. In either case, both the oral cavity balloon 406 and esophageal balloon 408 are deflated prior to insertion of the tubing and then inflated once oral cavity balloon 406 is within the oral cavity and esophageal balloon 408 is within, or near the esophagus. Nose block 426 may then be placed on the nose to block the nasal airway. A syringe (not shown) is connected to the inflation tubes 514 and 614. Using the syringe, air is then pumped through inflation tubes 514 and 614 and into oral cavity balloon 406 and esophageal balloon 408, respectively, until the oral cavity balloon 406 completely occludes the oral cavity so that air cannot exit. An Ambu-bag, or other hand-held device capable of providing positive pressure ventilation, is attached to the proximal end 640 of esophageal tube 403. The care provider then ventilates the patient by compressing the bag to pump air through esophageal tube 403 and into the trachea via aperture 412.

FIG. 8 is a block diagram illustrating one embodiment of an airway management process. In one embodiment, process 800 may include positioning a tubular member within an airway of a mammal (block 802). The tubular member may be, for example, any of the previously discussed tubular members described in connection with airway management device 100, for example, tubular member 104. Process 800 may further include inflating an oral cavity balloon attached to a proximal portion of the tubular member, within an oral cavity of the mammal, so as to occlude the oral cavity (block 804). The oral cavity balloon may be, for example, oral cavity balloon 106 previously discussed in connection with airway management device 100. An esophageal balloon attached to a distal portion of the tubular member may further be inflated within an esophagus of the mammal, so as to occlude the esophagus (block 806). The esophageal balloon may be, for example, esophageal balloon 108 previously discussed in connection with airway management device 100. An air flow may then be delivered into a trachea of the mammal by introducing air into the tubular member and out an aperture formed within a portion of the tubular member near the trachea (block 808).

It is to be understood that any of the above described airway management devices can be packaged as a kit with each of the parts pre-assembled or unassembled and the balloons deflated. The kit may come in a variety of different sizes to accommodate a variety of different patients. For example, in one embodiment, the airway management device may be manufactured in six different sizes to accommodate the patient sizes within the following age ranges: newborn (<30 days), infants (1 month to 11 months), toddlers (1-3 years), young children (4-10 years), older children (11-14 years) and adolescents and adults (>15 years).

It is further to be understood that the airway management devices disclosed herein provides several advantages including: 1) more secure airway than BMV; 2) lower chance of aspiration than BMV; 3) preferred in facial trauma than BMV; 4) can be used with one hand with Ambu-bag (thus free one hand off of the paramedics); 5) lower skills than endotracheal intubation; 6) less time needed than endotracheal intubation; 7) prevents tongue from obstructing the airway; and 8) avoids problems associated with other devices using a oropharyngeal balloon, such as venous thrombosis, nerve plexus injury, compromise of carotid flow, and post-extubation swelling.

In addition, although the various balloons described herein are described as being manually inflatable balloons, such as with an inflation tube, it is contemplated that self-inflation balloons or cuffs may also be used. Representatively, balloons or cuffs that can be chemically inflated using CO₂may be used. In still further embodiments, the airway management device may include a CO₂detector (e.g. a test strip) that can be placed near an exit port of one or more of the tubes near the patient's mouth to ensure the device is properly positioned and ventilation is occurring properly.

In the preceding detailed description, specific embodiments are described. It will, however, be evident that various modifications and changes may be made thereto without departing from the broader spirit and scope of the claims. The specification and drawings are, accordingly, to be regarded in an illustrative rather than restrictive sense.

DEVICE TO SECURE AIRWAY DURING EMERGENCY CARE

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CROSS-REFERENCE TO RELATED APPLICATION

Provisional Applications (1)