INTUBATION DEVICE IMPROVEMENTS

BACKGROUND OF THE INVENTION

The present invention relates to improvements to an intubation device for use in an endotracheal intubation procedure.

DESCRIPTION OF THE PRIOR ART

Endotracheal intubation is the procedure through which a medical professional introduces a flexible plastic conduit, an endotracheal tube, generally through the mouth and into the trachea. This allows artificial ventilation, which is required when the breathing ability is compromised by an illness or injury in an emergency situation or is interfered by drug-induced depression during surgery. It is a universal procedure and is performed in the same fashion all over the world.

Every day thousands of intubations are performed by a diverse range of professionals, particularly anaesthetics specialists, intensivists, emergency physicians and pre-hospital medics and paramedics. However endotracheal intubation is a high risk procedure which can lead to death or disability, requires considerable skill and occasionally cannot be accomplished. Even to highly trained professionals, it is often difficult and sometimes unsuccessful. New specialised instruments and advanced techniques are continuously developing with the aim to facilitate this difficult procedure and ensure better success rates.

The aim of the operator is to successfully pass an endotracheal tube through the mouth, pharynx and larynx and into the trachea. The oropharyngeal passage is curved and narrow and ends at the entrance of both the larynx and the oesophagus. The tongue tends to fall back on to the pharynx when a patient is in supine position, the entrance of the larynx can vary in its position due to the particular anatomy of a patient and the epiglottis lies over the entrance of the larynx and usually needs to be moved to expose the glottic opening.

The operator needs to identify the vocal cords at the entrance of the larynx, the epiglottis above the entrance of the larynx in the transversal view with the patient supine, and the oesophagus, below all previous structures on this view. This procedure requires extraordinary skills; it is easier for the endotracheal tube to follow the path towards the oesophagus, it is often difficult to obtain a good view of the larynx, and even with a good view, it is difficult sometimes to introduce the endotracheal tube. Any delay in successfully finalising the procedure is a serious complication, and may potentially be fatal.

The insertion of an endotracheal tube through all these anatomical structures and into the trachea is referred to as endotracheal intubation and typically requires the use of an instrument called laryngoscope. FIG. 1 shows an example of a prior art laryngoscope 1 which comprises a handle 2, and a blade 3. Different shapes of the blade 3 may be used depending on a range of factors such as the age or size of the patient and different procedural options. Laryngoscope blades are generally classified as curved or straight, although a number of styles of curved and straight blades are commercially available. Some styles of blades are designed to be positioned anterior to the epiglottis, and other styles are designed to be positioned posterior to the epiglottis, leading to slightly different movements during the procedure. A light source may be provided at the tip of the blade 3 to illuminate the area beyond. The light source may be powered by batteries within the handle 2.

During endotracheal intubation, with the patient laying supine, the operator, standing at the top of the head of the patient, introduces the blade 3 of the laryngoscope 1 through the mouth and into the pharynx and manipulates anatomical structures such as the tongue and the epiglottis (depending on the particular patient and type of blade) to expose the entrance of the larynx. Then, under direct visualisation, the operator inserts the tip of the endotracheal tube into the larynx and advances it into the trachea. In the conventional and universal procedure, the operator typically utilises the left hand to hold the laryngoscope 1 by the handle 2 to position the blade 3 and utilises the right hand to carefully introduce the endotracheal tube, pushing it along side the laryngoscope blade 3 and into the visualised trachea.

Often, because of anatomical variations and challenges, and despite an adequate technique, direct visualisation is difficult. In most of these occasions, adequate visualisation could be obtained by manipulating some of the anatomical structures. Unfortunately, with the conventional laryngoscope and conventional procedure, the operator is utilising both hands and the hand being used to manually introduce the endotracheal tube cannot be used to manipulate anatomical structures to facilitate the procedure. Furthermore, a second operator could not have direct visual access to the entrance of the larynx to help manipulating these structures and will interfere with the vision of the first operator, as the mouth opening, through which the first operator is obtaining the view, is very limited and the operator performing the intubation procedure will usually be in the best viewing position.

Due to the degree of difficulty of the procedure itself, together with the seriousness of the potential complications, this procedure will only be performed by highly skilled professionals. This difficulty and serious complication risk have also meant that the procedure, and the instruments used to perform it, has essentially remained unchanged for decades. The physicians and other professionals who perform endotracheal intubations are unwilling to use new devices or to change the way this is conventionally done, given the difficulties and risks. A new intubation device therefore not only has to offer obvious procedural advantages in comparison to the conventional laryngoscopes, but also has to present similar characteristics in shape and weight and in its method of use, to facilitate adoption by operators already trained and comfortable in the use of conventional laryngoscopes in the often stressful circumstances of performing an intubation procedure.

WO2003047673 discloses an automatically operative medical insertion device and method including an insertable element which is adapted to be inserted within a living organism in vivo, a surface following element, physically associated with the insertable element and being arranged to follow a physical surface within the living organism in vivo, a driving subsystem operative to at least partially automatically direct the insertable element along the physical surface and a navigation subsystem operative to control the driving subsystem based at least partially on a perceived location of the surface following element along a reference pathway stored in the navigation subsystem. However, the automatic operation of this device requires a complex arrangement of hardware with a significantly different configuration to conventional laryngoscopes, resulting in a relatively large and costly device compared to conventional laryngoscopes.

U.S. Pat. No. 5,184,603 discloses an intubating instrument comprising a laryngoscopic blade having a rounded distal end adapted for introduction into a patient's throat to expose the laryngeal opening for endotracheal intubation; side walls formed integrally with the blade and forming an elongated channel for an endotracheal tube; the channel being adapted to retain the tube within the laryngoscopic blade during insertion and manipulation of the instrument and to accommodate forward displacement of the tube beyond the distal end; the blade having a proximal end having a first quick-connect coupling associated therewith; a support handle housing for supporting the blade; a second quick-connect coupling matable with the first quick-connect coupling disposed at the lowermost portion of the support handle housing; the first and second quick-connect couplings being adapted to be mechanically engaged to lock the blade to the handle housing in a predetermined angular relationship; an endotracheal tube driver mounted in the handle housing; a tube driver operatively associated with the handle housing and the blade and adapted to engage a proximal portion of an endotracheal tube in the channel and to advance the tube beyond the distal end of the blade to introduce the distal end of the tube into the trachea; a finger-activated trigger mounted on the handle housing and adapted to initiate operation of the tube driver, whereby the exposure of the glottic opening and the introduction of the endotracheal tube may be effected with one hand while holding the handle housing. However, the instrument disclosed in this document has a significantly different configuration compared to conventional laryngoscopes. The positioning of the tube driver in particular is detrimental to the ergonomics of the instrument and may interfere with operator movements or anatomical structures during a procedure.

U.S. Pat. No. 5,776,052 discloses a laryngoscope that has a handle including a mechanism adapted to engage and advance a flexible fiberoptic tube of a bronchoscope. The mechanism is operated by the hand that grasps the handle. The laryngoscope has a blade extending from the handle which defines a surface extending from the handle to the distal end of the blade. The mechanism includes a guide which overlies the surface to define a channel through which the fiberoptic tube is advanced to the distal end of the blade. The mechanism is positioned to advance the flexible fiberoptic tube through the channel. The mechanism also displaces the guide from the surface allowing the laryngoscope to be removed from the flexible fiberoptic tube. However, the laryngoscope disclosed in this document only provides a mechanism for advancing a fiberoptic tube, not an endotracheal tube.

WO2011119521 discloses a fiberoptic intubating device which permits visualization of the vocal cords and automatic deployment of an endotracheal tube into the trachea upon visualization. The device includes a housing, a handle extending from the housing, and an extendable and retractable stylet extending from the distal end generally in parallel with the longitudinal axis. The device also includes a support member disposed on the housing that is configured to support the endotracheal tube with respect to the housing and to be selectively movable in the longitudinal direction relative to the housing. The device is configured to automatically move the stylet relative to the housing upon actuation of a trigger. Once the stylet is positioned relative to the vocal cords, the device is configured to deploy the endotracheal tube into the trachea upon further actuation of the trigger. However, the device disclosed in this document lacks a laryngoscope blade and has a significantly different configuration and operational ergonomics compared to conventional laryngoscopes.

WO/2016/090435A1 discloses a new intubation device that allows an endotracheal intubation procedure to be performed using a single hand. In particular, the intubation device includes: a laryngoscope blade having a tip and a base; a handle attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a channel for receiving an endotracheal tube, the channel including a blade channel portion extending along the blade substantially from the tip to the base and including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet and a handle channel portion extending partially along the handle from the blade channel portion; and a tube movement mechanism in the handle for moving the endotracheal tube through the channel to thereby advance the endotracheal tube, the tube movement mechanism including a thumb interface for allowing the user to operate the tube movement mechanism using a thumb of the hand that is holding the intubation device, to thereby allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand. The entire contents of WO/2016/090435A1 are incorporated herein by reference.

By enabling single handed operation of the intubation device for positioning the blade via the handle and advancing the endotracheal tube, the other hand of the user will remain free for other uses, such as clearing the airway using another device, such as a suction device, or other devices such as forceps or the like to manipulate anatomical structures and/or the endotracheal tube, during the endotracheal intubation procedure as may be required.

However, continued development of the single handed intubation device has led to improvements or alternative design variations for providing enhanced functionality.

The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that the prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.

SUMMARY OF THE PRESENT INVENTION

In one broad form an aspect of the present invention seeks to provide an intubation device for use in an endotracheal intubation procedure, the intubation device including: a laryngoscope blade having a tip and a base; a handle attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a channel for receiving an endotracheal tube, the channel extending along the blade and partially along the handle, and the channel including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet; a tube movement mechanism in the handle for moving the endotracheal tube through the channel to thereby advance the endotracheal tube, the tube movement mechanism being configured to allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand; and an auxiliary conduit for allowing an auxiliary function to be provided using the intubation device.

In one embodiment, the auxiliary function includes causing an object to be at least one of: delivered via the auxiliary conduit; advanced through the auxiliary conduit; and retracted through the auxiliary conduit.

In one embodiment, the auxiliary conduit extends at least partially along the blade, and the auxiliary conduit includes an auxiliary outlet proximate to the tip for allowing the object to pass through the auxiliary outlet.

In one embodiment, the auxiliary conduit further extends at least partially along the handle.

In one embodiment, the object is one of: an endoscope; a probe; a tube; a manipulator; and an electrode.

In one embodiment, a blade conduit portion of the auxiliary conduit that extends along the blade is at least one of: located posteriorly relative to the channel; and located laterally relative to the channel.

In one embodiment, the auxiliary outlet is oriented so that the object can extend from the auxiliary outlet at an angle relative to the endotracheal tube.

In one embodiment, the auxiliary conduit extends partially along the handle and connects to a proximal end of the channel within the handle for allowing the object to pass through the endotracheal tube.

In one embodiment, the object is one of: a bronchoscope; a bougie; a probe; a tube; a manipulator; and an electrode.

In one embodiment, the auxiliary conduit is looped within the handle.

In one embodiment, the auxiliary conduit includes an auxiliary inlet at a proximal end of the auxiliary conduit for allowing the object to be introduced into the auxiliary conduit via the auxiliary inlet.

In one embodiment, the auxiliary inlet passes through one of the blade and the handle.

In one embodiment, the intubation device includes an auxiliary movement mechanism for moving the object through the auxiliary conduit.

In one embodiment, the auxiliary function includes causing a fluid to be delivered via the auxiliary conduit.

In one embodiment, the fluid includes an at least one bioactive agent.

In one embodiment, the at least one bioactive agent includes at least one of: an anesthetic agent; a paralytic agent; a sedative agent; a bronchodilator agent; adrenaline; and an antiseptic agent.

In one embodiment, the auxiliary conduit extends at least partially along the blade, and the auxiliary conduit includes one or more auxiliary outlets located on the blade for allowing the fluid to be delivered via the one or more auxiliary outlets.

In one embodiment, the auxiliary conduit further extends at least partially along the handle.

In one embodiment, the auxiliary conduit is coupled to a reservoir for storing the fluid.

In one embodiment, the reservoir is one of: located inside the handle; and provided separate from the device.

In one embodiment, the intubation device includes a fiber optic cable extending along the auxiliary conduit.

In one embodiment, the intubation device includes a display for displaying images transmitted by the fiber optic cable.

In one embodiment, the auxiliary function includes causing an electrical signal to be transmitted via the auxiliary conduit.

In one embodiment, the electrical signal is one of: a sensor signal received from a sensor; an actuator signal for activating an actuator; and a bioelectrical stimulus signal for transmission to a subject.

In one embodiment, the intubation device includes an auxiliary control for activating the auxiliary function.

In one embodiment, the intubation device includes: a first digit interface for allowing the user to operate the tube movement mechanism using a digit of the hand that is holding the intubation device; and a second digit interface for allowing the user to activate the auxiliary function using a digit of the hand that is holding the intubation device.

In one embodiment, the intubation device is configured to allow the user to hold the intubation device, advance the endotracheal tube, and activate the auxiliary function using a single hand.

In another broad form an aspect of the present invention seeks to provide an intubation device for use in an endotracheal intubation procedure, the intubation device including: a laryngoscope blade having a tip and a base; a handle attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a channel for receiving an endotracheal tube, the channel extending along the blade and partially along the handle, and the channel including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet; a tube movement mechanism in the handle for moving the endotracheal tube through the channel to thereby advance the endotracheal tube, the tube movement mechanism being configured to allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand; a first digit interface for allowing the user to operate the tube movement mechanism using a digit of the hand that is holding the intubation device; and a second digit interface for allowing the user to activate an auxiliary function using a digit of the hand that is holding the intubation device.

In one embodiment, the intubation device includes an auxiliary conduit for allowing an auxiliary function to be provided using the intubation device.

In one embodiment, the auxiliary function includes causing an object to be at least one of delivered, advanced and retracted via the auxiliary conduit, the intubation device includes an auxiliary movement mechanism for moving the object through the auxiliary conduit, and the second digit interface is for activating the auxiliary movement mechanism.

In one embodiment, the auxiliary function includes causing a fluid to be delivered via the auxiliary conduit, and the second digit interface is for controlling the delivery of the fluid.

In one embodiment, the auxiliary function includes causing an electrical signal to be transmitted via the auxiliary conduit.

In one embodiment, the auxiliary function includes causing the endotracheal tube to be disengaged from the tube movement mechanism.

In one embodiment, the tube movement mechanism includes clips for engaging the endotracheal tube, the clips being configured to disengage the endotracheal tube in response to activation of the second digit interface.

In one embodiment, the blade includes a moveable blade portion and the second digit interface is for causing movement of the moveable blade portion.

In one embodiment, the moveable blade portion is configured so that movement of the moveable blade portion varies at least one of: a position of the tip of the blade; an angle of at least a distal portion of the blade proximate to the tip; and a curvature of the blade.

In one embodiment, the moveable blade portion and the second digit interface are configured so that activation of the second digit interface causes the moveable blade portion to move so that the curvature of the blade is increased.

In one embodiment, the moveable blade portion includes a plurality of articulated blade segments.

In one embodiment, the second digit interface is a lever.

In one embodiment, the intubation device includes a moveable manipulator and the second digit interface is for causing movement of the moveable manipulator.

In one embodiment, the moveable manipulator extends from one of: the tip of the blade; a distal portion of the blade proximate to the tip; and an intermediate portion of the blade between the tip and the handle.

In another broad form an aspect of the present invention seeks to provide an intubation device for use in an endotracheal intubation procedure, the intubation device including: a laryngoscope blade having a tip and a base; a handle attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a channel for receiving an endotracheal tube, the channel extending along the blade and partially along the handle, and the channel including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet; a tube movement mechanism in the handle for moving the endotracheal tube through the channel to thereby advance the endotracheal tube, the tube movement mechanism being configured to allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand; and a manipulator arrangement including: a moveable manipulator attached to the blade; a manipulator actuator for moving the manipulator; and a manipulator control in the handle, the manipulator control being configured to allow the user to operate the manipulator control using the same single hand.

In another broad form an aspect of the present invention seeks to provide an intubation device for use in an endotracheal intubation procedure, the intubation device including: a housing defining: a laryngoscope blade portion having a tip and a base; a handle portion attached to the base of the blade portion for allowing the intubation device to be held in a hand of a user; a conduit for receiving an endotracheal tube, the conduit extending along the blade portion and partially along the handle portion, and the conduit including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet; and a tube movement mechanism in the handle for moving the endotracheal tube through the conduit to thereby advance the endotracheal tube, the tube movement mechanism being configured to allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand.

In one embodiment, the housing is configured to be split along the conduit to allow the endotracheal tube to be removed from the conduit.

In one embodiment, the housing is at least one of: disposable; and reusable.

It will be appreciated that the broad forms of the invention and their respective features can be used in conjunction, interchangeably and/or independently, and reference to separate broad forms is not intended to be limiting.

BRIEF DESCRIPTION OF THE DRAWINGS

Various examples and embodiments of the present invention will now be described with reference to the accompanying drawings, in which: —

FIG. 1 is a side view of a prior art laryngoscope;

FIG. 2A is a perspective view of a first example of an intubation device;

FIG. 2B is a perspective view of the intubation device of FIG. 2A loaded with an endotracheal tube and showing a typical positioning of a user's thumb in use;

FIG. 2C is a perspective view of the intubation device of FIG. 2B showing the user's thumb operating a thumb interface to advance the endotracheal tube;

FIG. 2D is a detailed perspective view of the user's thumb operating the thumb interface to advance the endotracheal tube as shown in FIG. 2C;

FIG. 2E is a detailed perspective view of a coupling between the thumb interface and the endotracheal tube as shown in FIG. 2D;

FIG. 2F is a detailed perspective view of the coupling as shown in FIG. 2E showing advancement of the coupling following operation of the thumb interface;

FIG. 2G is a detailed perspective view of the coupling as shown in FIG. 2F showing disengagement of the endotracheal tube from the coupling;

FIG. 3A is a perspective view of an example of a user using the intubation device of FIG. 2A to perform an endotracheal intubation procedure on a subject;

FIG. 3B is a cross section view of the intubation device and the subject of FIG. 3A once the endotracheal tube has been placed into the trachea of the subject and removed from the intubation device;

FIG. 4 is a perspective view of a second example of an intubation device having an alternative form of the thumb interface;

FIG. 5 is a perspective view of a third example of an intubation device having a further alternative form of the thumb interface;

FIG. 6A is a perspective view of a fourth example of an intubation device in an operational configuration;

FIG. 6B is a perspective view of the intubation device of FIG. 6A in a collapsed configuration;

FIG. 6C is a perspective exploded view of the intubation device of FIG. 6A;

FIG. 6D is a perspective view of the intubation device of FIG. 6A showing the thumb interface in an advanced position;

FIG. 6E is a further perspective view of the intubation device of FIG. 6A showing the thumb interface in an advanced position;

FIG. 6F is a perspective view of the intubation device of FIG. 6A loaded with an endotracheal tube;

FIG. 6G is a perspective view of the intubation device and endotracheal tube of FIG. 6F following advancement of the endotracheal tube;

FIG. 7 is a schematic view of an example of an intubation device that is configured to deliver an endoscope and an endotracheal tube;

FIG. 8 is a schematic view of an example of an intubation device that is configured to deliver a bronchoscope and an endotracheal tube;

FIGS. 9A to 9D are schematic views of an example of an intubation device that is configured to deliver a bougie and an endotracheal tube, in which the bougie and the endotracheal tube are in different respective stages of advancement;

FIG. 10A is a schematic view of an example of an intubation device that includes an atomiser;

FIG. 10B is a schematic view of an example of an intubation device that includes a suction line;

FIG. 10C is a schematic view of an example of an intubation device that includes an atomiser and a suction line;

FIG. 11A is a schematic view of an example of an intubation device including a removable video subassembly;

FIGS. 11B and 11C are schematic views of the intubation device of FIG. 11A, in which the removable video subassembly is in different stages of removal;

FIGS. 12A and 12B are schematic views of an example of an intubation device including a moveable manipulator arm, in which the manipulator arm is in different positions;

FIG. 13A is a schematic view of an example of an intubation device including a detachable channel seal;

FIG. 13B is a schematic view of the intubation device of FIG. 13A with the detachable channel seal detached and showing a cuff seal surrounding the endotracheal tube;

FIG. 13C is a schematic view of the intubation device of FIG. 13B with the endotracheal tube displaced from the channel and the cuff seal;

FIGS. 14A to 14C are schematic views of an example of an intubation device similar to the intubation device of FIGS. 13A to 13C but further including an inflatable cuff seal;

FIG. 15A is a schematic view of an example of an intubation device that is configured to be split to allow removal of an endotracheal tube;

FIG. 15B is a schematic view of split segments of the intubation device of FIG. 15A;

FIG. 16 is a schematic view of an example of an intubation device including a transparent blade portion;

FIG. 17 is a schematic view of an example of an intubation device including a lever for operation by a digit of a user;

FIGS. 18A and 18B are schematic views of an example of an intubation device including a moveable blade portion, in which the blade portion is in different positions;

FIG. 19 is a schematic view of an example of an intubation device having a straight handle configuration; and

FIG. 20 is a schematic view of an example of an intubation device having a reverse curved handle configuration.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

An example of an intubation device 100 for use in an endotracheal intubation procedure will now be described with reference to FIGS. 2A to 2G.

With regard to FIG. 2A, the intubation device 100 includes a laryngoscope blade 110 having a tip 111 and a base 112. A handle 120 is attached to the base 112 of the blade 110 for allowing the intubation device 100 to be held in a hand of a user.

The intubation device 100 also includes a channel 101 for receiving an endotracheal tube 210, as shown in FIG. 2B. The channel 101 includes a blade channel portion 113 extending along the blade substantially from the tip 111 to the base 112, and a handle channel portion 123 extending partially along the handle 120 from the blade channel portion 113. The blade channel portion 113 includes an outlet 114 proximate to the tip 111 for allowing a distal end 211 of the endotracheal tube 210 to be advanced from the outlet 114, as shown in FIG. 2C.

The intubation device 100 further includes a tube movement mechanism 130 in the handle 120 for moving the endotracheal tube 210 through the channel 101 to thereby advance the endotracheal tube 210. The tube movement mechanism 130 includes a thumb interface 131 for allowing the user to operate the tube movement mechanism 130 using a thumb 201 of the hand that is holding the intubation device 100 (as shown in FIGS. 2B to 2F), to thereby allow the user to hold the intubation device 100 and advance the endotracheal tube 210 during an endotracheal intubation procedure using a single hand.

With reference to FIG. 3A, it will be seen that the user can hold the intubation device 100 by the handle 120 in a hand 301 with the thumb 201 of that hand being positioned for operation of the thumb interface 131. The user can manoeuvre the blade 110 relative to anatomical structures inside oropharyngeal passage of the patient 310 using the handle 120, to move the tip 111 of the blade 110 into position for advancement of the endotracheal tube 210. Once the tip 111 is suitably positioned, the user can then operate the thumb interface 131 to cause the tube movement mechanism to move the endotracheal tube 210 through the channel 101 and advance the endotracheal tube 210 into the trachea of the patient 310.

By enabling single handed operation of the intubation device 100 for positioning the blade 110 via the handle 120 and advancing the endotracheal tube 210, the other hand 302 of the user will remain free for other uses, such as clearing the airway using another device, such as a suction device 303, or other devices such as forceps or the like to manipulate anatomical structures and/or the endotracheal tube 210, during the endotracheal intubation procedure as may be required. It will be appreciated that the use of a single hand only can also help in avoiding visual obstructions during the procedure which would otherwise be presented if the endotracheal tube was to be manually advanced as per conventional procedures.

The general arrangement of the blade 110 and the handle 120 will be familiar to users experienced in performing endotracheal intubation procedures with conventional laryngoscopes, such that a suitably skilled user would be able to intuitively hold the handle 120 and manipulate the blade 110 during the procedure via the handle 120 in a generally conventional manner. However, the tube movement mechanism 130 within the handle 110 additionally provides the user with the capability of advancing the endotracheal tube 210 simply by operating the thumb interface 131. With a suitably configured and positioned thumb interface 131, the user can cause the endotracheal tube 210 to be advanced during the procedure using intuitive thumb movements, and whilst continuing to hold the intubation device 100 by the handle 120 with a grip similar to that used for conventional laryngoscopes.

Accordingly, it is expected that skilled users of conventional laryngoscopes would be able to use the intubation device 100 without requiring significant alteration to the way the user would hold and manipulate a conventional laryngoscope during an endotracheal intubation procedure. The main difference in performing the procedure will be operating the thumb interface 131 with the thumb of the hand holding the handle 110 to advance the endotracheal tube 210, rather than using their other hand to manually advance the endotracheal tube 210 as per conventional techniques.

However, it is noted that the user of the intubation device 100 may optionally perform an endotracheal intubation procedure in a completely conventional way using the intubation device 100, without using the thumb operated tube movement mechanism 130. For instance, the user may opt to use a more familiar conventional approach of manually advancing the endotracheal tube 210 alongside the blade 120 rather than through the channel 101, and the intubation device 100 may be configured to permit this use. This may be useful in a difficult intubation in which the user is unable to successfully position the endotracheal tube 210 using the thumb interface 131 and tube movement mechanism 130. The user may withdraw the endotracheal tube 210 from the channel 101 and manually insert the same endotracheal tube 210 so that it is guided by a surface of the blade 120. Alternatively, in a more urgent scenario the user may manually introduce a second endotracheal tube 210 alongside the blade 120 in a similar manner.

In some embodiments, the intubation device 100 may be configured to allow the user to readily transition from using the thumb interface 131 and tube movement mechanism 130 to advance the endotracheal tube 210 to manual advancement of the endotracheal tube 210, if this should be required. For example, a proximal end portion of the endotracheal tube 210 may be displaced from the channel 101 to allow the user to use their other hand to manually move the endotracheal tube 210 along the channel 101 to manually advance the endotracheal tube 210. This may be facilitated, for example, by configuring the channel 101 to allow displacement of the proximal end portion of the endotracheal tube 210 from the handle channel portion 123 whilst having another portion of the endotracheal tube 210 still retained within the blade channel portion 113.

In any event, it will be appreciated that providing the option to use manual advancement techniques, to thereby use the intubation device 100 like a conventional laryngoscope, can be helpful in increasing the confidence of a user adopting the use of the intubation device 100 in the place of a conventional laryngoscope. Despite this, it is expected that users will readily adopt the use of the thumb operated tube movement mechanism 130 due to its ease of use and the significant advantage of allowing single handed operation, freeing up the user's other hand for other activities.

The tube movement mechanism 130 and its thumb interface 131 can be provided in different forms depending on requirements. In one form, the tube movement mechanism 130 is directly coupled to the thumb interface 131 so that a movement of the thumb interface 131 results in an equivalent movement of the endotracheal tube 210 through the channel 101. In another form, the tube movement mechanism 130 may be configured to convert a movement of the thumb interface 131 into a longer movement of the endotracheal tube 210. In some examples, the tube movement mechanism 130 includes an actuator which is controlled by the thumb interface 131.

It will be appreciated that the arrangement of the channel 101 to extend along the blade 110 and partially along the handle 120 allows a proximal end 212 of the endotracheal tube 210 to be located in the handle channel portion 123. Thus, the proximal end 212 may be positioned in the handle 120 in proximity to the tube movement mechanism 130 provided in the handle 120. It will be appreciated that this can result in an arrangement in which the tube movement mechanism 130 may be completely contained within the handle 120 and engage with the proximal end 212 of the endotracheal tube 210 to thereby move the endotracheal tube 210 through the channel 101 without any external protrusions from the handle 120 or the blade 110, that could otherwise interfere with anatomical structures or the movements of the user during the procedure. Preferred forms of the intubation device 100 will thus allow the user to go about the same movements of the hand holding the handle 120 as if the user was using a conventional laryngoscope, without interference by structures of the device. Accordingly, the channel 101 configuration including the handle channel portion 123 and the provision of the movement mechanism 130 within the handle 120 further facilitates the ability to provide the intubation device 100 in a familiar form which can be readily adopted by users experienced with the use of conventional laryngoscopes.

Turning back to the example embodiment of the intubation device 100 depicted in FIG. 2A, other optional features will now be described.

The blade 110 may be formed with a similar overall shape as conventional laryngoscope blades such as that depicted in FIG. 1. As with conventional laryngoscope blades, the blade 110 may be provided in different sizes and with different shapes (e.g. straight or curved blades 110, blades 110 with different degrees of curvature, blades 110 with straight or curved tips 111), to suit different ages, sizes and shapes of patients, different oropharyngeal anatomies or different procedural options. The blade 110 may be configured in accordance with traditional curved laryngoscope blade styles (such as the “Macintosh” blade style) or straight laryngoscope blade styles (such as the “Miller” blade style).

In some examples, the blade 110 may be detachable from the handle 120. This can allow the use of different blades 110 as required whilst having a single handle 120 and tube movement mechanism 130 provided within. A first end 121 of the handle 120 may thus include a coupling arrangement for allowing the base 112 of a blade 110 to be coupled to or detached from the handle 120. The intubation device may be configured to allow the attachment of different blades 110 having different shapes and sizes, depending on requirements for the endotracheal intubation procedure.

It will be appreciated that this will allow the intubation device 100 to be used in a range of different circumstances by attaching a blade 110 with a suitable shape for the patient and the procedural option selected by the user. The coupling arrangement may utilise similar coupling techniques as for conventional laryngoscopes to allow the blade to be attached and detached in a manner that is familiar to users with experience using conventional laryngoscopes. For example, the blade 110 and the handle 110 may be provided with complementary bayonet coupling interfaces, or any other suitable style of coupling interfaces. It should be noted, however, that the coupling arrangement should ensure proper alignment between the blade channel portion 113 and the handle channel 123 when the blade 110 is attached to the handle 120, to thereby form a continuous effective channel 101.

The blade 110 and the handle 120 may be formed from any material suitable for use in medical devices. In some examples, the blade 110 and the handle 120 may be formed from moulded plastic components, which can allow for relatively inexpensive manufacture. The blade 110 and/or the handle 120 may even be provided as disposable items to avoid the need for sterilisation following a procedure. In such examples, it may be preferable to provide the tube movement mechanism 130 components in a simple and low-cost form. However, reusable versions of the handle may be provided with a more sophisticated tube movement mechanism 130, and only the blade 110 which comes into contact with the patient might be disposed of. Alternatively, reusable metal components may be used to provide the blade 110 and the handle 120 as is often the case for conventional laryngoscopes.

The thumb interface 131 may be mounted near a second end 122 of the handle 120 for appropriate positioning relative to the user's hand when gripping the handle 120. In this example, the handle 120 has an ergonomic grip 124 for allowing the user to comfortably yet securely hold the handle 120 during use.

In this example intubation device 100, the thumb interface 131 is provided in the form of a thumb slider, such that the thumb interface 131 is operated by the user slidingly moving the thumb slider using the thumb of the user. The thumb slider of the thumb interface 131 slides along a slot 125 formed in the handle 120, and the thumb interface 131 is mechanically coupled to internal components of the tube movement mechanism 130 within the handle 120 via the slot 125. Further details of the tube movement mechanism 130 and operation of the thumb interface 131 will be provided in due course with reference to illustrative usage examples.

It should be appreciated that a range of different thumb interface 131 arrangements other than that depicted in FIG. 2A may be used. For example, FIG. 4 shows an example of an intubation device 400 including press buttons 431, 432 as the thumb interface 131, and FIG. 5 shows another example of an intubation device 500 including a thumb wheel 531 as the thumb interface 131. Different types of thumb interfaces 131 may be coupled to the tube movement mechanism 130 in different ways as will be discussed further in due course.

In this example, the channel 101 is defined along posterior faces of the blade 110 and the handle 120. The blade 110 may include a tissue engaging anterior blade face (being the face of inside curvature for a curved style of blade 110 as depicted in the Figures) and an opposing posterior blade face, and the handle 120 may include a posterior handle face extending from the posterior blade face. The blade channel portion 113 and the handle channel portion 123 may be respectively defined in the posterior blade face and the posterior handle face. The channel 101 will thus provide an elongate opening extending along the posterior faces of the blade 110 and the handle 120. Once the endotracheal tube 210 has been positioned using the intubation device 100, the endotracheal tube 210 may be removed from the elongate opening channel 101 by pulling the endotracheal tube 210 in an outward direction relative to the intubation device 100, in this case posteriorly.

However, in other examples, the channel 101 may be defined along lateral faces of the blade 110 and the handle 120, adjacent to the posterior faces. Accordingly, whilst the path of the channel 101 may follow the shape of the posterior faces of the blade 110 and the handle 120, the elongate opening of the channel 101 may be offset to a side of the intubation device 100. This arrangement can allow the endotracheal tube 210 to be removed from the elongate opening channel 101 by pulling the endotracheal tube 210 in an outward direction relative to the intubation device 100, in this case laterally. This lateral positioning of the elongate opening of the channel may allow the user to remove the endotracheal tube 210 from the intubation device 100 using the user's other hand while maintaining a constant grip on the handle 120 with the first hand.

In the depicted embodiment of the intubation device 100, the posterior handle face and the posterior blade face collectively define a continuously curved posterior face of the intubation device 100, with the channel 101 being defined in this curved posterior face (although as noted above, in other embodiments the channel 101 may be defined in a lateral face adjacent to this curved posterior face). In this case, the curved posterior face is rounded along each of the blade 110 and the handle 120. However, this is not essential and the respective posterior faces of the blade 110 and the handle 120 may include straightened portions, such as in the case of a blade 110 with a straight laryngoscope blade type.

The channel 101 may define a curved passageway for receiving the endotracheal tube 120. By forming the channel 101 in or adjacent to a curved posterior face, this allows the channel 101 to provide a suitable passageway whilst maintaining a consistent depth relative to the posterior faces. Despite this, the channel 101 may be formed with variable depth to provide a suitable curved passageway for the endotracheal tube 120 for posterior face geometries that are not curved or rounded.

The intubation device 100 may include retention tabs 115, 116, 117, 126 partially covering sections of the elongate opening of the channel 101, for retaining the endotracheal tube 210 within the channel 101. The retention tabs 115, 116, 117, 126 may be provided as extensions of the above discussed faces across the elongate opening of the channel 101, and act to prevent unintentional dislocation of the endotracheal tube 210. The number, shapes and locations of the retention tabs 115, 116, 117, 126 may vary depending on the intubation device geometry and usage requirements, although in this case there are three retention tabs 115, 116, 117 provided for the blade channel portion 113, and a single retention tab 126 provided for the handle channel portion 123.

The retention tabs 115, 116, 117, 126 are preferably configured to prevent the endotracheal tube 210 from being displaced from the channel 101 unless the endotracheal tube 210 is positively removed by a user. Endotracheal tubes 210 are typically be formed from a flexible material, so the retention tabs 115, 116, 117, 126 may be configured to require some deformation of the endotracheal tube 210 when locating the endotracheal tube 210 into the channel or removing the endotracheal tube 210 from the channel.

The retention tabs 115, 116, 117, 126 should generally retain the endotracheal tube 210 in the channel 101 without allowing significant radial movement. For a channel 101 defined in posterior faces of the blade 110 and the handle 120, as per the depicted example, the retention tabs 115, 116, 117, 126 should prevent the endotracheal tube 210 from being displaced outwardly from the channel 101 under normal movements of the intubation device 100, unless the user positively removes the endotracheal tube 210 by pulling it outwardly in a posterior direction from the intubation device 100. In other examples having the channel 101 defined in lateral faces of the blade 110 and the handle 120, the retention tabs 115, 116, 117, 126 should prevent the endotracheal tube 210 from being displaced outwardly in a lateral direction from the channel 101 unless under a positive user action for removing the endotracheal tube 210.

The endotracheal tube 210 may be provided with a pre-curved configuration so that it is urged against the blade 110 and the handle 120 and easy to locate into the channel 101 without requiring the retention tabs 115, 116, 117, 126 to provide significant retaining force on the endotracheal tube 210.

The intubation device 100 may also include a light source 140 located proximate to the tip 111 of the blade 110, for providing illumination during the procedure.

In some examples, the intubation device 100 may further include a fiber optic viewing arrangement for allowing the user to observe anatomical structures inside the patient without requiring a direct view. The fiber optic viewing arrangement may include a flexible fiber optic bundle with a lens positioned at one end proximate to the tip 111 of the blade 110 and an eyepiece positioned at the other end. The fiber optic bundle may run along the blade 110 and into the handle 120. The eyepiece may be located on the handle 120 or on a suitably formed projection from the handle 120 to allow the user to look into the eyepiece during the procedure.

In other examples, the intubation device 100 may include a video camera located proximate to the tip 111 of the blade 110, for providing video imaging of anatomical structures inside the patient during the procedure. It will be appreciated that this can provide even more flexible viewing options compared to the fiber optic viewing arrangement discussed above. The video camera may be connected to a display for displaying images from the video camera in real-time or near real-time during the procedure. Whilst a small display may be integrated with the intubation device 100, it may be preferable to provide a separate large display for displaying magnified images of the internal anatomical structures, in a more convenient viewing location for the user. The connection to the display may be achieved via a cable extending from the intubation device 100 or via a wireless communications connection which can avoid interference of user movements by a cable.

In some embodiments, the intubation device 100 may include a suction channel having a suction outlet proximate to the tip 111 of the blade 110. The suction channel may be configured to receive a suction tube to allow suction at the suction outlet. This can remove the need for the user to use a separate suction device with the other hand while using the intubation device 100.

The operation of example embodiment of the intubation device 100 depicted in FIG. 2A will now be described in further detail with reference to the subsequent FIGS. 2B to 2G.

As shown in FIG. 2B, the intubation device 100 may be loaded with an endotracheal tube 210, by placing the endotracheal tube 210 in the channel 101 with the distal end 211 of the tube positioned at the outlet 114 of the channel 101 near the tip 111 of the blade 110. The proximal end 212 of the endotracheal tube 210 will be positioned near the end of the blade channel portion 123 within the handle 120. The endotracheal tube 210 may be placed into the channel 101 by pushing the endotracheal tube 210 into the elongate opening of the channel 101 past the retention tabs 115, 116, 117, 126, either from a posterior or lateral direction relative to the intubation device 100 depending on how the channel 101 is defined. Alternatively, the endotracheal tube 210 may be inserted through the outlet 114 and passed along the channel 101, although this may only be possible if the endotracheal tube 210 is not provided with a tube fitting 220 or the like at its proximal end. In either case, the endotracheal tube 210 should be located substantially inside the channel 101 as shown in FIG. 2B.

The tube movement mechanism 130 may include a tube engager 132 (visible in FIGS. 2C to 2G) for engaging the proximal end 212 of the endotracheal tube 210 located in the handle channel portion 123 and causing the endotracheal tube 210 to move through the channel 101 in response to operation of the thumb interface 131. The thumb interface 131 may be coupled to the tube engager 132 so that a movement of the thumb interface 131 by the thumb of the user causes a corresponding movement of the endotracheal tube 210 through the tube channel.

In a simple form, the tube engager 132 may simply be provided as a member that abuts the proximal end 212 of the endotracheal tube 210 to allow the tube movement mechanism 130 to move the endotracheal tube 210 by pushing the tube engager 132 within the handle channel portion. However, providing the tube engager 132 in such a way will only allow for movement of the endotracheal tube 210 in a direction that advances the endotracheal tube 210.

Accordingly, in the depicted embodiment of the intubation device 100, the tube engager 132 is configured to provide for movement in two directions, to thereby allow advancement and retraction of the endotracheal tube 210. The thumb interface 131 may thus be moveable in opposing first and second directions, such that a movement of the thumb interface 131 in the first direction advances the endotracheal tube 210 and a movement of the thumb interface 131 in the second direction retracts the endotracheal tube 210.

In this example the tube engager 132 is provided in the form of a clip arrangement which allows pushing and pulling forces to be applied to the proximal end 212 of the endotracheal tube 210. Further features of the tube engager 132 will be discussed with regard to subsequent Figures, in due course.

In any event, the thumb interface 131 may be coupled to the tube engager 132 so that a movement of the thumb interface 131 by the thumb of the user causes a corresponding movement of the endotracheal tube 210 through the tube channel 101.

FIG. 2C shows the intubation device 100 and endotracheal tube 210 after the thumb interface 131 has been moved by the user's thumb 201 in a direction as indicated by arrow 202. This movement of the thumb interface 131 has caused a corresponding movement of the tube engager 132 and in turn the endotracheal tube 210, as indicated by arrow 203. As a result, the distal end 211 of the endotracheal tube 210 is advanced from the outlet 114 as indicated by arrow 204.

FIGS. 2D and 2E show progressively closer details of the handle 120 and interface between the tube movement mechanism 130 and the proximal end 212 of the endotracheal tube 210 within the handle channel portion 123. In this example, the tube engager 132 engages with a connector fitting 220 that is fitted to the proximal end 212 of the endotracheal tube 210. The connector fitting 220 may be designed specifically for use with the intubation device 100, although more preferably the connector fitting 220 will be a standard type of tube connector and the tube engager 132 will be configured to provide a suitable interface.

Turning to the more detailed view of FIG. 2E, it will be seen that the connector fitting 220 includes a first connector end 221 that is connected to the proximal end 212 of the endotracheal tube 210 and an opposing second connector end 222, which may be adapted for connection to further tubing coupled to assisted breathing apparatus or the like. In this example, the connector fitting 220 also includes a flange 223 between the first and second connector ends 222, as is commonly the case for standard endotracheal tube connector fittings.

The tube engager 132 of this embodiment of the intubation device 100 is configured to interface with the flange 223 to thereby facilitate movement of the endotracheal tube 210. In particular, the tube engager 132 clips on to the flange 223 to allow the tube engager 132 to push or pull on the flange 223 when the tube engager 132 moves in response to operation of the thumb interface. However, it should be appreciated that a range of alternative tube engager 132 configurations may be used.

FIG. 2F shows a similar view to FIG. 2E after the thumb interface 131 has been moved in the direction of arrow 205 for the full extent of movement allowed by the slot 125. This represents the maximum extend of advancement of the endotracheal tube using the tube movement mechanism 130 in this case. In this state, the tube engager 132 has fully extended into the handle channel portion 123 and it can be seen that the clips of the tube engager 132 are attached to the tube mechanism 130 within the handle by links 133, which may be formed from wire or another suitably rigid material for transferring loads to the tube engager 132.

In this example, the thumb interface 131 is mechanically coupled to the tube movement mechanism 130 so that a movement of the thumb interface 131 is mechanically translated into a corresponding movement of the endotracheal tube 210. In a simple form of the tube movement mechanism 130, the tube engager 132 may be directly coupled to the thumb interface 131, such as by connecting the links 133 directly between the thumb slide of the thumb interface 131 and the tube engager 132. This will result in the amount of movement of the endotracheal tube 210 being equivalent to the amount of movement of the thumb interface. However, this may lead to a large range of thumb movement being required to complete an endotracheal intubation procedure.

Accordingly, in alternative examples, the tube movement mechanism 130 may be configured so that a movement of the thumb interface 131 by a thumb movement distance translates into a movement of the endotracheal tube 210 by a tube movement distance which is greater than the thumb movement distance. In other words the intubation device may allow a relatively small thumb movement to translate into a larger tube movement.

Typically there will be a proportional relationship between the thumb movement and the resulting tube movement. The tube movement distance may be related to the thumb movement distance by a multiplication factor provided by mechanical advantage in the tube movement mechanism. For instance, the tube movement mechanism may include a lever arrangement or a gear train configured to multiply the movement of the thumb interface 131. It will be appreciated that such arrangements may allow for a smaller range of thumb movement to be used to advance the endotracheal tube 210. This could help to prevent thumb fatigue during intubation procedures, or simply allow for more comfortable operation.

Although a mechanical tube movement mechanism 130 can provide a relatively simple and low cost capability for translating movement of the thumb interface 131 into movement of the endotracheal tube 210, alternative forms of the tube movement mechanism 130 may include an actuator (not shown) for moving the endotracheal tube 210, the actuator being activated in response to operation of the thumb interface 131. For example, the actuator may be in the form of an electric motor coupled to a suitable tube engager 132 via a rack and pinion arrangement or the like for providing linear movement of the endotracheal tube 210. The actuator may be electrically powered by a battery, which may be housed within the handle along with the actuator and any other tube movement mechanism 130 components.

In versions of the intubation device 100 including an actuator, the tube movement mechanism 130 may be configured so that operation of the thumb interface 131 causes a control input to be provided to the actuator, for controlling the activation of the actuator.

Accordingly, the use of an actuator may allow for the use of different styles of thumb interfaces which accept different forms of input from the user's thumb. For example, the thumb interface may include a press button, such that a control input is provided to the actuator when the press button is pressed by the thumb of the user. In further examples, the thumb interface may include a plurality of press buttons for each providing different control inputs to the actuator when pressed by the thumb of the user. The alternative intubation device 400 of FIG. 4 shows an example of an arrangement with two press buttons 431, 432 for advancing and retracting the endotracheal tube 120, respectively.

In an example of another different form of the thumb interface 131, the further alternative intubation device 500 of FIG. 5 shows an example in which the thumb interface 131 includes a thumb wheel 531, such that the thumb interface is operated by the user rolling the thumb wheel using the thumb of the user. The thumb wheel 531 may either be mechanically coupled to tube engager 532, such as by way of a gear train, belt arrangement or the like, or may be connected to a suitable sensor for generating a control input when the thumb wheel is rolled.

Turning back to FIG. 2G, it will be appreciated that the tube engager 132 in this example allows the proximal end 212 of the endotracheal tube 210 to be disengaged after the endotracheal tube 210 has been successfully advanced. In particular, the user may grip the flange 223 between the user's thumb 201 and a finger 206 and remove this from the clips of the tube engager 132 by moving the tube connector 220 in the direction indicated by arrow 207.

As shown in the cross section view of FIG. 3B, the user can then proceed to remove the endotracheal tube 210 from the channel 101, past the retention tabs 115, 116, 117, 126, so that the intubation device 100 can be removed from the mouth 311 of the patient 310 while leaving the endotracheal tube 210 in position within the patient's trachea 312.

It is noted that the endotracheal tube 210 in this example includes a balloon 213 which can be inflated after successful intubation to seal the tracheal passage around the endotracheal tube 210. The endotracheal tube 210 also includes an inflation conduit 320 for allowing the balloon 213 to be inflated. The channel 101 and its outlet 114 should be sized accordingly, to accommodate the balloon 213, inflation conduit 320, and other optional features of the endotracheal tube 210.

Further general discussion of suitable embodiments of the intubation device 100, along with suitable methods of their use and associated advantages, are provided below.

In view of the above, it will be appreciated that of the intubation device 100 may be provided in the form of a laryngoscope-like device with a generally conventional size and shape.

One difference in shape between the example intubation device 100 and conventional laryngoscopes is that the posterior face of the device is typically curved or rounded along the handle 120 and the blade 110. In particular, the intubation device 100 may include a handle 120 that outwardly differs from conventional laryngoscopes in the shape of the posterior face, which is curved or rounded instead of linear. This curved or rounded face is continued on the posterior face of the blade 110, which may be attached to the handle 120 in a similar manner as in the conventional laryngoscope. Both of the curved or rounded faces, namely the posterior faces of the handle 120 and the blade 110, may create a continuously curved portion. In some embodiments this continuously curved portion may be in the form of a continuous semicircle.

Along this curved or rounded posterior face, the channel 101 is defined for locating the endotracheal tube 210 before being inserted into the trachea of the subject. Retention tabs 115, 116, 117, 126 in the form of non-complete borders along both sides of the channel 101 may prevent the endotracheal tube 210 from being displaced laterally from the channel 101 until it is manually separated laterally in a positive action by the user (usually once the distal end 211 is allocated inside the trachea 312). Those borders maintain the endotracheal tube 210 inside the channel 101 while it is moved forward but do not prevent the endotracheal tube 210 from being removed laterally, as they only partially close the channel 101 laterally.

In some examples, the endotracheal tube 210 may be grasped with a pin in a superior part of the channel 101 within the handle 120, and this pin may be connected with a thumb interface 131 in the form of a mechanical switch that can be activated with the thumb of the hand that is holding the intubation device 100. By moving the thumb down and up over the switch the endotracheal tube 210 is moved down and up through the channel 101. The thumb interface 131 will typically be located over the rounded posterior face of the handle 120, preferably on a superior area of the handle, so it can be easily reached with the thumb of the hand that is holding the intubation device 100.

Other features of the intubation device 100 may be common to those found in conventional laryngoscopes. For example, embodiments of the intubation device 100 may include a power source and a light source 140 at the tip 111 of the blade 110. The blade 110 may be formed separately from the handle 120 and may be interchangeable using a bayonet mounting, so different sizes and types can be used, depending on patient anatomy and operator preferences.

The endotracheal tube 210 can be introduced through the trachea by positioning the tip 211 of the endotracheal tube 210 in alignment with the entrance of the larynx as shown in FIG. 3B and advancing the endotracheal tube 210 through the channel 101 inside the intubation device 100 by moving the thumb of the same hand that is holding the intubation device 100. The user utilises the intubation device 100 in a similar fashion as for a conventional laryngoscope, to hold the tongue and facilitate the visualisation of the entrance to the larynx.

Once this has been achieved the user aligns the tip 211 of the endotracheal tube 210 with the entrance of the larynx so the endotracheal tube 210 can be introduced with the movement of the same hand's thumb. This technique requires only a single hand, as opposed to a conventional endotracheal intubation procedure, leaving the other hand of the user free to help remove obstacles and facilitate the way of the endotracheal tube into the trachea.

The user also has the ability to move the endotracheal tube 210 backwards with an opposite movement of the thumb on the switch of the thumb interface 131, so a failed advance of the endotracheal tube 210 can be corrected and the operation can be started again until the correct placement of the endotracheal tube 210 in the trachea 312 is achieved.

Once the tip of the endotracheal tube 210 has been introduced through the vocal cords into the larynx and it has been advanced into the trachea 312, the proximal end 212 of the endotracheal tube 210 is detached from the pin that previously held it, followed by the whole endotracheal tube 210 being detached from the channel 101 along the handle 120 and the blade 110 of the intubation device. Then, while leaving the endotracheal tube 210 in the desired place, the intubation device 100 is removed from the mouth and pharynx of the patient, as in the conventional procedure.

The fact that the other hand of the user is left free represents a significant advantage, as this hand can be utilised to manipulate anatomical structures which often impend the access to the larynx. Typically only the user is able to see such obstructions, and, with the intubation device 100, the user is also able to manipulate them to facilitate the endotracheal intubation procedure. This results in a significant improvement of the technique for endotracheal intubation, which can significantly improve the success rate of this difficult procedure.

The depicted embodiment of the intubation device 100 intentionally has a similar size and shape compared to conventional laryngoscopes, except for the curved or rounded posterior face and channel 100 for the endotracheal tube 210. By being similar otherwise to the conventional laryngoscopes, the professionals used to them can start to use this new device and procedure safely, being perfectly familiar with the general procedure up to the point of the insertion of the endotracheal tube 210, and knowing that at any time they can decide to use this device as a normal laryngoscope and proceed to intubate in the conventional way.

In this regard, the intubation device 100 will preferably be configured to allow the user to disengage the proximal end 212 of the endotracheal tube 210 from the tube movement mechanism 130 and remove from the channel 101 at least a portion of the endotracheal tube 210 near the proximal end 212, to facilitate manual advancement should this be required. It will be appreciated that this can be enabled by appropriately positioning the retention tabs 115, 116, 117, 126, particularly the retention tab 126 in the handle channel portion 123.

A further example of an intubation device 600 will now be described with regard to FIGS. 6A to 6G. It should be noted that features similar to those of the previous example of the intubation device 100 have been assigned similar reference numerals, increased by 500.

With initial regard to FIG. 6A, it will be seen that the intubation device 600 has an overall configuration generally similar to the previous intubation device examples. The intubation device 600 includes a laryngoscope blade 610 having a tip 611 and a base 612. A handle 620 is attached to the base 612 for allowing the intubation device 600 to be held in a hand of a user.

As per the previous examples, the intubation device 600 also includes a channel 601 for receiving an endotracheal tube 210, as shown in FIG. 6F. The channel 601 includes a blade channel portion 613 extending along the blade 610 substantially from the tip 611 to the base 612, and a handle channel portion 623 extending partially along the handle 620 from the blade channel portion 613. The blade channel portion 613 includes an outlet 614 proximate to the tip 611 for allowing a distal end 211 of the endotracheal tube 210 to be advanced from the outlet 114, as shown in FIG. 6G. In this example, the blade channel portion 613 and the handle channel portion 623 are respectively defined in a lateral blade face and a lateral handle face, and thus the channel 601 includes an elongate opening extending along the lateral blade face and the lateral handle face.

The intubation device 600 further includes a tube movement mechanism 630 in the handle 620 for moving the endotracheal tube 210 through the channel 601 to thereby advance the endotracheal tube 210. The tube movement mechanism 630 includes thumb interfaces 631 for allowing the user to operate the tube movement mechanism 630 using a thumb of the hand that is holding the intubation device 600, as previously described, to thereby allow the user to hold the intubation device 600 and advance the endotracheal tube 210 during an endotracheal intubation procedure using a single hand.

This example of the intubation device 600 may also include a range of optional features as discussed with regard to previous examples. For instance, the intubation device 600 includes a light source 640 for providing illumination during the intubation procedure, as best seen in FIG. 6E.

In this example, the intubation device 600 is formed as an assembly of parts as best seen in the exploded view of FIG. 6C. The assembly includes separate parts providing the blade 610, the handle 620 and the tube movement mechanism 630, along with a cap 650 and a battery insert 660. The base 621 of the blade 610 is attached to the handle 620 at a first end 621 of the handle 620. The tube movement mechanism 630 is inserted into a second end 622 of the handle 620 and positioned in a slot 625 extending from the second end 622 of the handle 620. The cap 650 closes the second end 622 of the handle 620 and may be secured in position using a ball detent arrangement, where the ball 651 can be seen in FIG. 2C and the detent 624 can be seen in FIG. 6E. It will be appreciated that other methods of securing the cap 650 in position relative to the handle 620 may be used, such as by providing a suitable threaded fastener.

The battery insert 660 is provided to house and provide an electrical connection for a battery 670 for supplying power to the light source 640. In this example, the battery insert 660 receives a button cell battery 670 as shown in FIG. 6A and can inserted into a suitably defined receptacle inside the handle 620. FIG. 6A shows the position of the battery insert 660 after insertion into the handle 620 receptacle. The battery insert 660 is inserted via an opening 602 defined in the handle 620. As will be discussed in due course, this opening 602 is also used to load the endotracheal tube 120 into the intubation device 600 and remove the endotracheal tube 120 from the intubation device 600. The battery insert 660 may also include a low battery warning light 663 that is visible from outside the handle when the battery insert 660 is inserted into the receptacle.

The intubation device 600 is configured so that the blade 610 is hingedly connected to the first end 621 of the handle 620. This hinged connection is achieved using a hinge pin 619 provided at the base 612 of the blade 610, which is received in a complimentary hinge socket 629 at a first end 621 of the handle 620. The blade 610 is secured in an operational configuration as shown in FIG. 6A using a ball detent arrangement, where at least one ball 628 is provided on the first end 621 of the handle 620 and at least one corresponding detent 618 is provided on the base 612 of the blade 610. However, the ball detent arrangement can be disengaged by positive manual action to cause the blade 610 to swing about the hinge pin 619 into a collapsed configuration as shown in FIG. 6B.

Furthermore, in this example, the blade 610 can be detached from the handle 620 by detaching the hinge pin 619 from the hinge socket 629 when the blade 610 is in the collapsed configuration. It will be appreciated that a range of different sizes and shapes of blades 610 may be provided for attachment to the intubation using this form of hinged connection. Therefore the same handle 620 and other associated parts including the tube movement mechanism 630, the cap 650 and the battery insert 660 can be used in intubation procedures with different blades 610 selected to suit the anatomy of patient. For instance, whilst the depicted example shows a curved “Macintosh” blade style, a straight “Miller” blade style may be used, and different sizes may be selected depending on the age, size and/or weight of the patient.

In this example, the blade channel portion 613 extends along a curved path from the tip 614 to the base 612 of the blade 610 and retention tabs 615, 617 are provided for retaining the endotracheal tube 210 within the blade channel portion 613 in use as can be seen in FIGS. 6F and 6G, with their functionality being similar as discussed for equivalent features in the previous examples.

The handle channel portion 623 extends between the opening 602 and the first end 621 of the handle 620, and continues the curved path of the blade channel portion 613 into the handle 620. The blade channel portion 613 and the handle channel portion 623 together define a continuous curved channel 601 within which the endotracheal tube 210 is received as shown in FIGS. 6F and 6G.

As described in previous examples, the endotracheal tube 210 is advanced by having the user operate the tube movement mechanism 630, particularly by interacting with a thumb interface 631 using a thumb of the same hand that is holding the handle 620 of the intubation device 600. In this example, the tube movement mechanism 630 includes a plurality of thumb interfaces 631 positioned at regular intervals along an elongate member 634 that extends from a tube engager 632 for receiving the endotracheal tube 210.

The tube engager 632 is configured to interface with the flange 223 of the endotracheal tube 210 in a similar manner as described above for the earlier example of the intubation device, to thereby facilitate movement of the endotracheal tube 210. As can be seen in FIG. 6D, the tube engager 632 includes a pair of curved clips 633, 633 which define a slot 634 therebetween. Now referring to FIG. 6G, which shows the endotracheal tube 210 loaded into the intubation device 600 and advanced to reveal the tube engager 632, the flange 223 is inserted into the slot 634 and the clips 633, 635 respectively engage the connector ends 221, 222 of the endotracheal tube 210. This positively engages the endotracheal tube 210 so that the endotracheal tube 210 moves along with the tube movement mechanism 630 when it is operated by the user's thumb via one of the thumb interfaces 631.

In this example, each thumb interface 631 is provided in the form of a generally trapezoidal protrusion extending outwardly from the elongate member 634, although it will be appreciated that the shape of the protrusion can vary depending on requirements. In use, the user will engage their thumb with one of the thumb interfaces 631 and push the thumb interface to move the elongate member 634 along the slot and thereby use the tube movement mechanism 630 to move an endotracheal tube 210 loaded into the intubation device. Faces of the thumb interfaces 631 may have ribs or other textured finishes for enhancing engagement of the thumb interfaces 631 by the thumb of a user.

It should be appreciated that the use of multiple thumb interfaces 631 can allow a greater range of movement of the tube movement mechanism 630 without needing the user to reposition their hand or over extend their thumb. Rather, when the user reaches a limit of their thumb movement, the user can use their thumb to engage a more suitably positioned thumb interface 631 and continue moving the tube movement mechanism 630 using that thumb interface 631. This process may be iterated several times to fully advance the endotracheal tube. It should be appreciated the thumb interfaces 631 can be used to move the tube movement mechanism 630 in a reversed direction to retract the endotracheal tube 210 during the intubation procedure if required, for instance if a first intubation attempt is unsuccessful. Following such a retraction, the intubation device 600 may be reoriented or repositioned relative to the patient's anatomy and the tube movement mechanism 630 may be moved in the advancing direction to thereby advance the endotracheal tube 210 once again.

The elongate member 634 of the tube movement mechanism 630 is received in the slot 625 and allowed to slide along the slot 625 as the thumb interfaces 631 are operated. The slot 625 may extend along the length of the handle 620, and as can be seen in FIGS. 6F and 6G, the intubation device 600 may be designed so that the tube movement mechanism 630 is able to slide along the length of the handle 620, to enable a significant amount of thumb-operated advancement of the endotracheal tube 210, without any requirement of sophisticated mechanisms to provide mechanical advantage to multiply the thumb movement distance. In some examples, the handle 620 may include a pocket that effectively extends the slot 625 inside the handle 620 to allow an even greater range of movement of the tube movement mechanism 630 in the advancing direction.

It may be desirable to provide a relatively long elongate member 634 having many thumb interfaces 631 to enable a correspondingly long range of movement of the tube movement mechanism 630 without requiring overextension of the user's thumb. However, the range of movement of the tube movement mechanism 630 will be limited by the length of the slot 625 and the above mentioned pocket (if provided). In some embodiments, this may be mitigated to some extent by forming at least the elongate member 634 (and potentially a greater portion or the entirety of the tube movement mechanism 630) from a flexible material and/or by using a hinged construction, so that the elongate member 634 is capable of compressing or collapsing inside the slot 625 (or pocket) after abutting a stop at the end of the slot 625 (or pocket). Thus the user may continue to advance the endotracheal tube 210 even after an end of the elongate member 634 reaches the end of the slot 625 (or pocket).

As mentioned previously, the opening 602 is used to allow the endotracheal tube 210 to be loaded into or removed from the intubation device 600, as best appreciated with reference to FIG. 6G. The opening 602 will typically be sized to receive the flange 223 and the connector ends 221, 222 of the endotracheal tube 210 and allow these to be engaged with the tube engager 632 of the tube movement mechanism 630 when in an advanced position as shown in FIGS. 6D and 6E. A portion of the endotracheal tube 210 extending from the connector ends 221, 222 is loaded into the channel 601, with the retention tabs 615, 617 retaining the intubation tube 210 inside the blade channel portion 623. The endotracheal tube 210 can then be retracted by moving the tube movement mechanism 630 into a retracted position as shown in FIG. 6F, with the distal end 211 of the endotracheal tube 210 positioned proximate to the outlet 614 of the blade 610.

At this stage the endotracheal tube 210 is loaded into the intubation device 600 and ready for use in an endotracheal intubation procedure. During the procedure, the user operates the tube movement mechanism 630 by engaging their thumb with the thumb interfaces 631 as need to advance the endotracheal tube 210 from the outlet 114, as shown in FIG. 6G. When the endotracheal tube 210 has been successfully advanced into a suitable position within the patient, the flange 223 and the connector ends 221, 222 of the endotracheal tube 210 will typically be aligned with the opening 602, and may be disengaged from the tuber engager 632, after which the proximal end 212 of the endotracheal tube may be removed from the opening 602 by the user. The remainder of the endotracheal tube 210 will similarly be removed by displacing it from the channel 601, so that the intubation device 600 can be withdrawn with the endotracheal tube 210 in position within the patient.

Although the user may simply use another hand to pull the proximal end 212 of the endotracheal tube 210 from the opening 602, in this example an access hole 603 is also provided in the handle 620 opposite to the opening 602 for allowing the user to access the proximal end 212 endotracheal tube 210 from the other side and push the endotracheal tube 210 through the opening 602. The access hole 603 may be positioned to allow the user to extend through the access hole 603 a finger from the same hand that is holding the device, to thereby enable one-handed disengagement of the endotracheal tube 210 from the tube engager 632 to facilitate removal of the endotracheal tube 210. For example, the user may extend their index finger through the access hole 603 and push the proximal end 212 of the endotracheal tube 210 out of the opening 602, all whilst maintaining the user's grip on the handle 620. Following this, the user may manipulate the endotracheal tube 210 with other fingers of the same hand to further disengage and remove the endotracheal tube 210 from the channel 601.

It will be appreciated that the above described example of the intubation device 600 allows a large range of movement of the endotracheal tube 210 while using a relatively simple tube movement mechanism 630 which can be comfortably operated by the user's thumb whilst simultaneously holding the intubation device 600 with the same hand. This example also provides for easier loading and removal of the endotracheal tube 210 using the opening 602 and the access hole 603, respectively. The detachable hinged connection of the blade 210 to the handle 220 also provides increased flexibility in terms of storage in the collapsed position and the capability of using a wide range of different blade types and sizes.

In one envisaged scenario, the intubation device 600 may be used to intubate a patient while the patient is being supplied with oxygen via a mask that includes a suitably configured orifice for allowing insertion of the intubation device 600, without any interruption of the supply of oxygen to the patient during the intubation procedure. In this case, the intubation device 600 may be provided with seals (not shown) across at least part of the channel 601 and the openings 602, 603 to thereby substantially prevent air from escaping from the mask via the intubation device 600. In one example, the seals may be configured to snap onto the channel portions 613, 623 and opening 602, 603 and be removable to allow disengagement of the endotracheal tube 210 after successful intubation.

Whilst the above examples, have primarily discussed operation of the intubation device using a thumb of the same hand that is holding the device, it will be appreciated that the intubation device may be adapted for operation using any digit of the user's hand, including the thumb or any finger Although thumb operation is considered to provide the most natural action for advancing the endotracheal tube with the same hand that is holding the device, one or more fingers could be used to operate the tube movement mechanism with a reversed grip, or an alternative form of the intubation device may be provided with the tube movement mechanism reconfigured for operation using one or more fingers as opposed to a thumb.

Accordingly, in one example, there may be provided an intubation device for use in an endotracheal intubation procedure, the intubation device including: a laryngoscope blade having a tip and a base; a handle attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a channel for receiving an endotracheal tube, the channel including a blade channel portion extending along the blade substantially from the tip to the base and including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet, and a handle channel portion extending partially along the handle from the blade channel portion; and a tube movement mechanism in the handle for moving the endotracheal tube through the channel to thereby advance the endotracheal tube, the tube movement mechanism including a digit interface for allowing the user to operate the tube movement mechanism using one or more digits of the hand that is holding the intubation device, to thereby allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand.

It will be appreciated that the operation of such an intubation device configured for operation by one or more digits of the same hand that is holding the device may have fundamentally similar design features as the above described examples. However, if the intubation device is specifically adapted for operation by one or more fingers as opposed to the thumb, this may necessitate reconfiguration and/or repositioning of the digit interface compared to the thumb interface of the previous examples. Nevertheless, the principle of one-handed operation may generally be the same.

The intubation device 600 as discussed above may alternatively be used to perform a bougie-assisted endotracheal intubation procedure. A bougie is an elongate flexible device with a relatively small diameter compared to a standard endotracheal tube 210 and an angled tip at its distal end, and may be used to facilitate endotracheal intubation in difficult circumstances, such as where a patient's anatomy does not permit adequate visibility or prevents insertion of a standard endotracheal tube 210.

In a conventional bougie-assisted endotracheal intubation procedure, the bougie may be inserted into the patient's trachea using a traditional laryngoscope, with the angled tip assisting in guiding the bougie through the patient's anatomical structures. Once the bougie is correctly positioned, the laryngoscope can be withdrawn and an endotracheal tube 210 is threaded over the bougie, and then passed along the bougie to thereby advance the endotracheal tube 210 so it is guided along the path the bougie has taken through the patient's anatomy. Following advancement of the endotracheal tube 210 into a suitable position, the bougie can be extracted leaving only the endotracheal tube 210, such that the endotracheal intubation procedure is complete.

It will be appreciated that the intubation device 600 may be used in place of a traditional laryngoscope to facilitate the insertion of the bougie in a bougie-assisted intubation procedure. To enable this, some small alterations to a standard bougie may be required to make the bougie compatible with the intubation device 600. These alterations may include shortening the length of the bougie to fit along the channel 601 of the intubation device 600 and providing a suitable connector fitting 220 on a proximal end of the bougie opposing the angled distal end, to thereby allow the bougie to be engaged by the tube engager 632 of the tube movement mechanism 630 of the intubation device 600. The connector fitting 220 will preferably be of the same configuration as used for the endotracheal tube 210, so that the tube engager 632 can engage the connector fitting 220 of the bougie in the same manner as the connector fitting 220 of the endotracheal tube 210.

Accordingly, in one example the intubation device may be provided for use in a bougie-assisted endotracheal intubation procedure, the intubation device including: a laryngoscope blade having a tip and a base; a handle attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a channel for receiving a bougie, the channel including a blade channel portion extending along the blade substantially from the tip to the base and including an outlet proximate to the tip for allowing a distal end of the bougie to be advanced from the outlet and a handle channel portion extending partially along the handle from the blade channel portion; and a tube movement mechanism in the handle for moving the bougie through the channel to thereby advance the bougie, the tube movement mechanism including a thumb interface for allowing the user to operate the tube movement mechanism using a thumb of the hand that is holding the intubation device, to thereby allow the user to hold the intubation device and advance the bougie in a bougie-assisted endotracheal intubation procedure using a single hand.

The method of operating the intubation device 600 for inserting a bougie in a bougie-assisted intubation procedure will be essentially the same as described above for a standard intubation procedure using an endotracheal tube, with the only difference being that the bougie is loaded into and advanced from the intubation device 600 instead of the endotracheal tube 210. It will be appreciated that once the bougie has been successfully advanced and inserted into the correct position within the patient, an endotracheal tube 210 can be threaded onto and passed along the bougie in a conventional manner to thereby intubate the patient using the bougie as a guide. Once the endotracheal tube 210 has been suitably placed, the bougie can then be removed through the internal conduit of the endotracheal tube 210 to leave only the endotracheal tube 210 within the patient.

In some examples, specialized versions of the intubation device 600 may be provided that are particularly configured for use in a bougie-assisted endotracheal intubation procedure. For instance, the channel 601 may be sized to accommodate the bougie only, which could allow for a smaller blade to be used in difficult intubations. The tube engager 630 may also have a different configuration to engage with a different type of connector fitting 220 specifically adapted to the bougie. Despite this option, it would still be advantageous to allow the same intubation device 600 to be used with either a bougie or an endotracheal tube 210, depending on the particular circumstances of an endotracheal intubation procedure. It will be appreciated that if an attempted intubation procedure using the intubation device 600 an endotracheal tube 210 is unsuccessful, the user could then attempt a bougie-assisted endotracheal intubation procedure using the same intubation device 600 but with a bougie instead of the endotracheal tube 210.

In summary, the intubation device may provide a direct replacement for a conventional laryngoscope that allows intubation with a single hand. This intubation device 100 therefore allows a new method for intubation. Since the size and the shape of the intubation device may be similar to conventional laryngoscopes, this will allow not only familiarity and easy adaptation to the new method, but also, if decided, the option to proceed as in the conventional method of intubation, with minimal differences perceived.

It will be appreciated that this is a particularly beneficial aspect, since endotracheal intubation is a high risk procedure and the process of change to a new procedure needs to be safe. For the same reason, a new intubation device 100 and procedure for endotracheal intubation will only be accepted and adopted by the professionals involved if the changes from the conventional device and procedure are minimised and, even better, if the new device allows at any point, to proceed as in the conventional procedure.

A number of improvements and/or alternative variations to the intubation devices discussed above will now be described.

In the examples to follow, it will be generally assumed the different improved embodiments of the intubation devices may be provided for use in a single handed endotracheal intubation procedure and may be based on the earlier described embodiments of the intubation device, as originally disclosed in WO/2016/090435A1. It is also noted that features of the improved intubation devices have been assigned reference numerals similar to those of the previously described example of the intubation device as shown in FIGS. 6A to 6G, where appropriate. However, it should be appreciated some of the improvements may also be implemented into other types of intubation devices, as will be noted where applicable.

Embodiments of the intubation device may be further improved to provide a user with the capability to perform one or more auxiliary activities to support or supplement the main intubation procedure. For instance, embodiments of the intubation device may be configured to provide one or more auxiliary functions alongside the primary function of enabling a single handed endotracheal intubation procedure as described above.

In some embodiments, the intubation device may include the core elements of: a laryngoscope blade having a tip and a base; a handle attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a channel for receiving an endotracheal tube, the channel extending along the blade and partially along the handle, and the channel including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet; and a tube movement mechanism in the handle for moving the endotracheal tube through the channel to thereby advance the endotracheal tube, the tube movement mechanism being configured to allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand, and additionally include an auxiliary conduit for allowing an auxiliary function to be provided using the intubation device.

As will be described in further detail below, the addition of an auxiliary conduit in this manner can be used to enable a range of different auxiliary functions to be provided in order to supplement the basic single handed intubation functionality of the device.

For instance, the auxiliary function may include causing an object to be delivered via the auxiliary conduit, advanced through the auxiliary conduit, or retracted through the auxiliary conduit.

In some particular embodiments, the auxiliary conduit may extend at least partially along the blade, and the auxiliary conduit may include an auxiliary outlet proximate to the tip for allowing the object to be delivered from the auxiliary outlet. Optionally, the auxiliary conduit may further extend at least partially along the handle. Examples of objects that may be delivered, advanced or retracted using such an auxiliary conduit configuration may include an endoscope (as per the device of FIG. 7), a probe, a tube, a manipulator (as per the device of FIGS. 12A and 12B), or an electrode.

In some examples, a blade conduit portion of the auxiliary conduit that extends along the blade may be located posteriorly relative to the channel, or located laterally relative to the channel. The auxiliary outlet may optionally be oriented so that the object can extend from the auxiliary outlet at an angle relative to the endotracheal tube.

In some other particular embodiments, the auxiliary conduit may extend partially along the handle and connect to a proximal end of the channel within the handle for allowing the object to pass through the endotracheal tube. Examples of objects that may be delivered, advanced, or retracted using such an auxiliary conduit configuration may include a bronchoscope (as per the device of FIG. 8), a bougie (as per the device of FIGS. 9A to 9D), a probe, a tube, a manipulator or an electrode. In some examples, the auxiliary conduit may be looped within the handle, to thereby enable objects longer than the handle to be provided within the auxiliary conduit.

The auxiliary conduit may optionally include an auxiliary inlet at a proximal end of the auxiliary conduit for allowing the object to be introduced into the auxiliary conduit via the auxiliary inlet. For instance, the auxiliary inlet may pass through the blade or the handle.

In some of the above discussed embodiments in which the auxiliary function includes causing an object to be delivered via the auxiliary conduit, the intubation device may further include an auxiliary delivery mechanism for moving the object through the auxiliary conduit.

A specific example of an improved intubation device 700 embodying an auxiliary conduit for delivering, advancing or retracting an object will now be described with reference to FIG. 7. In this case, the intubation device 700 is configured to provide an auxiliary function of advancing/retracting an endoscope via an auxiliary conduit.

As per previously described embodiments of the intubation devices, the intubation device 700 includes a laryngoscope blade 710 having a tip 711 and a base 712, a handle 720 attached to the base 712 of the blade 710 for allowing the intubation device 700 to be held in a hand of a user, a channel for receiving an endotracheal tube 210, and a tube movement mechanism 730 in the handle 720 for moving the endotracheal tube 210 through the channel to thereby advance the endotracheal tube 210. The channel extends along the blade 710 and partially along the handle 720, the channel includes an outlet proximate to the tip 711 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet, and the tube movement mechanism 730 is configured to allow the user to hold the intubation device 700 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

However, in this case, the intubation device 700 additionally includes an auxiliary conduit 780 for allowing an auxiliary function to be provided using the intubation device 700, specifically advancing or retracting an endoscope 790 via the auxiliary conduit 780. It will be appreciated that the capability to advance/retract an endoscope 790 using the delivery device 700 will provide a beneficial additional functionality to support the single handed delivery of an endotracheal tube. In use, the endoscope 790 may be advanced before advancing the endotracheal tube 210 to allow visualisation of the subject's anatomy before delivery of the endotracheal tube 210 into the subject's airway.

In this particular embodiment, the auxiliary conduit 780 extends along the blade 710, and includes an auxiliary outlet 781 proximate to the tip 711 for allowing the endoscope 790 to pass through the auxiliary outlet 781. The auxiliary conduit 780 also extends along the handle 720, and includes an auxiliary inlet 782 at a proximal end of the auxiliary conduit 780 for allowing the endoscope 790 to be introduced into the auxiliary conduit 780 via the auxiliary inlet 782. The auxiliary inlet 782 typically passes through one of the blade 710 and the handle 720, and in this case, the auxiliary inlet 782 passes through the cap 750 at the proximal end of the handle 720.

The endoscope 790 may be manually moved through the auxiliary conduit 780 as required to advance the endoscope tip 791 into the subject's airway as required before, during, or after the single handed delivery of the endotracheal tube 210. In some optional embodiments, the intubation device 700 may include an auxiliary movement mechanism (not shown in this example) for moving the endoscope 790 through the auxiliary conduit 780. In such embodiments, a separate control interface may be provided to allow the user to control the movement of the endoscope 790 using the auxiliary movement mechanism. It will be appreciated that this may allow the auxiliary function of advancing/retracting the endoscope 790 to also be controlled using a single hand.

In this example, a blade conduit portion of the auxiliary conduit 780 that extends along the blade 710 is located posteriorly and laterally relative to the channel. The auxiliary outlet 781 is also oriented so that the endoscope 790 extends from the auxiliary outlet 781 at an angle relative to the endotracheal tube 720. The specific location of the blade conduit portion and the auxiliary outlet 781 of the auxiliary conduit 780 may be selected to provide a suitable advancement trajectory for the endoscope 790 to suit the anatomy of subjects.

In any event, it will be appreciated that the intubation device 700 is only one example of a potential configuration for providing the auxiliary functionality of advancing/retracting an endoscope 790 via an auxiliary conduit 780 of the intubation device 700, and the specific configuration of the intubation device 700 may be varied in other embodiments that provide equivalent functionality.

Furthermore, it will be appreciated that similar configurations of the intubation device 700 may be used to provide other auxiliary functionalities, such as delivering, or advancing, or retracting other types of objects including a probe, a tube, a manipulator, or an electrode. For instance, an intubation device may be specifically configured to allow advancement of an electrode for providing an electrical stimulus to the internal anatomy of the subject, such as to enable oesophageal defibrillation which the subject is intubated.

Another example of an improved intubation device 800 embodying an auxiliary conduit for the delivering, advancing or retracting an object will now be described with reference to FIG. 8. In this example, the intubation device 800 is specifically configured to provide an auxiliary function of advancing/retracting a bronchoscope via an auxiliary conduit that extends partially through the handle portion of the intubation device and connects with the channel for allowing the bronchoscope to pass concentrically through the endotracheal tube.

Once again, as per previously described embodiments of the intubation devices, the intubation device 800 includes a laryngoscope blade 810 having a tip 811 and a base 812, a handle 820 attached to the base 812 of the blade 810 for allowing the intubation device 800 to be held in a hand of a user, a channel for receiving an endotracheal tube 210, and a tube movement mechanism 830 in the handle 820 for moving the endotracheal tube 210 through the channel to thereby advance the endotracheal tube 210. The channel extends along the blade 810 and partially along the handle 820, the channel includes an outlet proximate to the tip 811 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet, and the tube movement mechanism 830 is configured to allow the user to hold the intubation device 800 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

In this particular embodiment, the intubation device 800 also includes an auxiliary conduit 880 for allowing an auxiliary function to be provided using the intubation device 800, however in this case the intubation device 800 is specifically adapted to allow a bronchoscope 890 to be advanced or retracted through the auxiliary conduit 880 and the endotracheal tube 210. The functionality of advancing/retracting a bronchoscope 890 using the intubation device 800 can assist or supplement the main functionality of the intubation device 800 of single handed delivery of an endotracheal tube 210. In use, the bronchoscope 890 may be advanced through the endotracheal tube 210 to allow visualisation of the subject's airway before, during or after the delivery of the endotracheal tube 210 into the subject's airway.

In this particular embodiment, the auxiliary conduit 880 extends partially along the handle 820 and connects to a proximal end of the channel within the handle 820 for allowing the bronchoscope 890 to pass through the endotracheal tube 210. The bronchoscope 890 may effectively be threaded through both the auxiliary conduit 880 and the endotracheal tube 210 so that a tip 891 of the bronchoscope 890 may be advanced from the distal end 211 of the endotracheal tube 210.

In this case, the auxiliary conduit 880 also includes an auxiliary inlet 882 at a proximal end of the auxiliary conduit 880 for allowing the bronchoscope 890 to be introduced into the auxiliary conduit 880 via the auxiliary inlet 882. In this example, the auxiliary inlet 882 passes through the cap 850 at the proximal end of the handle 820.

As was the case for the endoscope 790 in the previous example, the bronchoscope 890 may be manually moved through the auxiliary conduit 880 as required to advance the bronchoscope tip 891 into the subject's airway as required before, during, or after the single handed delivery of the endotracheal tube 210. In some optional embodiments, the intubation device 800 may include an auxiliary movement mechanism (not shown) for moving the bronchoscope 890 through the auxiliary conduit 880 and endotracheal tube 210, which may be in a retracted or advanced state. Once again, a separate control interface may be provided to allow the user to control the movement of the bronchoscope 890 using the auxiliary movement mechanism, which can thus enable single handed activation of the auxiliary function.

As mentioned above, in some embodiments, the auxiliary conduit may be looped within the handle, to thereby enable objects longer than the handle to be provided within the auxiliary conduit. An example of an improved intubation device 900 embodying a looped auxiliary conduit will now be described with reference to FIGS. 9A to 9C. In this example, the intubation device 900 is specifically configured to provide an auxiliary function of advancing/retracting a bougie via an auxiliary conduit 980 that is looped inside the handle portion 920 of the intubation device 900 and, as per the previous example for advancing/retracting a bronchoscope 890, connects with the channel for allowing the bougie to pass concentrically through the endotracheal tube 210.

The intubation device 900 is similar to the previous example and includes a laryngoscope blade 910 having a tip 911 and a base 912, a handle 920 attached to the base 912 of the blade 910 for allowing the intubation device 900 to be held in a hand of a user, a channel for receiving an endotracheal tube 210, and a tube movement mechanism 930 in the handle 920 for moving the endotracheal tube 210 through the channel to thereby advance the endotracheal tube 210. The channel extends along the blade 910 and partially along the handle 920, the channel includes an outlet proximate to the tip 911 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet, and the tube movement mechanism 930 is configured to allow the user to hold the intubation device 900 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

In this particular embodiment, the intubation device 900 also includes an auxiliary conduit 980 for allowing an auxiliary function to be provided using the intubation device 900, however in this case the intubation device 900 is specifically adapted to allow a bougie 990 to be advanced or retracted via the auxiliary conduit 980 and the endotracheal tube 210. The bougie 990 can be advanced ahead of the endotracheal tube 210 using the intubation device 900, so that the bougie 990 can be passed through the subject's airway to a desired position and then used as a guide to facilitate easier delivery of the endotracheal tube 210.

The auxiliary conduit 980 extends partially along the handle 920 and connects to a proximal end of the channel within the handle 920 for allowing the bougie 990 to be delivered through the endotracheal tube 210. The bougie 990 may be threaded through both the auxiliary conduit 980 and the endotracheal tube 210 so that a tip 991 of the bougie 990 may be advanced from the distal end 211 of the endotracheal tube 210. In this case, the auxiliary conduit 980 is looped inside the handle 920 so that the length of the bougie 990 can be longer than the length of the handle 920. Depending on the number of loops, the auxiliary conduit 980 may accommodate a bougie 990 that is several times longer than the handle 920.

The bougie 990 may be manually moved through the auxiliary conduit 980 or moved using an auxiliary movement mechanism which may include a separate control interface which may be operable using the same hand that is holding the device, as discussed with regard to the examples above.

It is noted that FIGS. 9A to 9D show the intubation device 900 with the endotracheal tube 210 and the bougie 990 in different positions, reflective different stages of use of the intubation device 900, as will be briefly discussed below.

In FIG. 9A, the intubation device 900 has been preloaded with a bougie 990 entirely contained within the auxiliary conduit 980, in a looped configuration inside the handle 920. At this stage, the bougie 990 does not extend inside the endotracheal tube 210, which is initially placed in the channel of the intubation device 900 with the tube movement mechanism 930 in an advanced position.

In FIG. 9B, the tube movement mechanism 930 has been moved into a retracted position to thereby move the proximal end of the endotracheal tube 210 inside the handle 920, such that the distal end 211 of the endotracheal tube 210 is located inside the tip 911 of the blade 910 of the intubation device 900. At this stage, the bougie 990 will extend partially through the endotracheal tube 210.

In FIG. 9C, the bougie 990 is advanced through the endotracheal tube 210 so that the tip 991 of the bougie 990 protrudes from both the distal end 211 of the endotracheal tube 210 and the tip 911 of the blade 910 of the intubation device 900. As the bougie 990 is advanced, the user can direct the path of the bougie 990 by moving the handle 920 and blade 910 of the intubation device 900 as required.

It will be appreciated that the bougie 990, having a significantly slimmer profile compared to the endotracheal tube 210, will be easier for the user to successfully advance into the desired position within the subject's airway compared to the endotracheal tube 210, and therefore may be especially useful in difficult intubations, such as where the subject's airway is obstructed.

Then following positioning of the bougie 990, the endotracheal tube 210 can be advanced by moving the tube movement mechanism 930 as shown in FIG. 9D, so that the endotracheal tube 210 moves along the bougie 990 and is guided into the desired position. Once the endotracheal tube 210 has been successfully delivered, the bougie 990 can be retracted back into the intubation device 900, the endotracheal tube 210 can be displaced from the channel, and the intubation device 900 can be removed, leaving only the endotracheal tube 210 to provide an airway for the subject.

It will be appreciated that the above described intubation devices 800, 900 provide further examples of potential configurations for providing the auxiliary functionality of delivering, advancing or retracting an object such as a bronchoscope 890 or a bougie 990 via an auxiliary conduit 880, 980 and the endotracheal tube 210, but the specific configuration of the intubation device 800, 900 may be varied in other embodiments that provide equivalent functionality. It will again be appreciated that similar configurations of the intubation devices 800, 900 may be used to provide other auxiliary functionalities, such as delivering/advancing/retracting other types of objects including a probe, a tube, or an electrode, as discussed above.

In some alternative embodiments, the auxiliary function may include causing a fluid to be delivered via the auxiliary conduit. For instance, the fluid may include at least one bioactive agent, such as an anesthetic agent, a paralytic agent, a sedative agent, a bronchodilator agent, an adrenal agent and/or an antiseptic agent.

In examples of the delivery device that are adapted for fluid delivery as the auxiliary function, the auxiliary conduit may extend at least partially along the blade, and the auxiliary conduit may include one or more auxiliary outlets located on the blade for allowing the fluid to be delivered via the one or more auxiliary outlets. The auxiliary conduit may optionally further extend at least partially along the handle.

In some implementations, the auxiliary conduit may be coupled to a reservoir for storing the fluid. The reservoir may be located inside the handle or provided separate from the device, depending on the particular design.

A specific example of an improved intubation device 1001 embodying an auxiliary conduit for the delivery of a fluid will now be described with reference to FIG. 10A.

The intubation device 1001 includes a laryngoscope blade 1010 having a tip 1011 and a base 1012, a handle 1020 attached to the base 1012 of the blade 1010 for allowing the intubation device 1001 to be held in a hand of a user, a channel for receiving an endotracheal tube 210, and a tube movement mechanism 1030 in the handle 1020 for moving the endotracheal tube 210 through the channel to thereby advance the endotracheal tube 210. The channel extends along the blade 1010 and partially along the handle 1020, the channel includes an outlet proximate to the tip 1011 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet, and the tube movement mechanism 1030 is configured to allow the user to hold the intubation device 1000 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

In this example, the intubation device 1001 additionally includes an auxiliary conduit 1080 for allowing an auxiliary function to be provided using the intubation device 1001, specifically the delivery of a fluid via the auxiliary conduit 1080. It will be appreciated that the capability to deliver a fluid will provide a beneficial additional functionality to support the single handed delivery of an endotracheal tube. In use, the fluid may be delivered before, during or after advancing the endotracheal tube 210 to allow the fluid to be provided to the subject's anatomy as required during the procedure. For example, the fluid may be an anesthetic agent which may provide a local anesthetic effect in prior to the delivery of the endotracheal tube 210.

In this particular embodiment, the auxiliary conduit 1080 extends along the blade 1010 and includes a number of auxiliary outlets 1081 arranged along a portion of the blade 1010, for allowing the fluid to be delivered via the one or more auxiliary outlets 1081. The auxiliary outlets 1081 may be arranged proximate to the tip 1011, and may be provided on different regions of the blade 1010 depending on the target site of the subject's anatomy for delivery of the fluid. The shape and configuration of the auxiliary outlets 1081 may be varied depending on the particular fluid to be delivered. For example, size of the auxiliary outlets 1081 may be selected so that they deliver the fluid as a fine mist, or as droplets, or as a continuous flow, as required.

The auxiliary conduit 1080 may further extend at least partially along the handle 1020 as shown. The auxiliary conduit 1080 may be coupled to a reservoir (not shown) which may be located inside the handle 1020 for storing the fluid. In this example, the delivery device 1020 includes a fluid delivery interface 1082 that can be activated by the user to cause fluid to be delivered via the auxiliary conduit 1080. In one example, the fluid delivery interface 1082 may simply be a flexible sidewall of a reservoir for storing the fluid, whereby the user may activate the fluid delivery interface 1082 by applying pressure to the flexible sidewall of the reservoir and therefore pressurising the fluid stored within and causing some of the fluid to flow along the auxiliary conduit 1080 so that it can be delivered from the auxiliary outlets 1081 as required. The fluid delivery interface 1082 may be configured to allow activation by the same hand that is holding the intubation device 1000, thereby enabling the auxiliary function to be activated using the same hand in a similar manner as per the delivery of the endotracheal tube 120.

A similar delivery device configuration may be used to allow suction through the auxiliary conduit, as shown in the example delivery device 1002FIG. 10B. The delivery device 1002 of FIG. 10B has essentially the same configuration as for the previous example of FIG. 10A, except in this case, the delivery device 1002 includes a different type of auxiliary conduit 1090 specifically adapted for providing a suction capability to the delivery device 1002.

The auxiliary conduit 1090 also extends along the blade 1010 and includes a number of auxiliary outlets 1091 arranged along a portion of the blade 1010 as per the previous example, but in this example, the auxiliary conduit 1090 is for allowing fluids and materials to be drawn into the auxiliary outlets 1091 and conveyed along the auxiliary conduit 1090 under suction, when the auxiliary conduit 1090 is connected to a suction source. The auxiliary outlets 1091 may be arranged proximate to the tip 1011, and may be provided on different regions of the blade 1010 depending on where suction may be required.

The auxiliary conduit 1090 may further extend at least partially along the handle 1020 as shown, and in this case the auxiliary conduit 1090 includes an auxiliary inlet 1092 at a proximal end of the auxiliary conduit 1090 for allowing the auxiliary conduit 1090 to be connected to a suction source via suction tubing or the like. The auxiliary inlet 1092 may pass through the blade 1010 or the handle 1020, and in the example, of FIG. 10B, the auxiliary inlet 1092 is located midway along the handle 1020.

The example intubation device 1003 shown in FIG. 10C combines the functionalities of the two previous examples, by including both the auxiliary conduit 1080 for delivering a fluid as per the intubation device 1001 of FIG. 10A, and the auxiliary conduit 1090 for providing suction as per the intubation device 1002 of FIG. 10B.

As discussed for the examples, embodiments of the intubation device may be configured to allow the user to hold the intubation device, advance the endotracheal tube, and activate the auxiliary function using a single hand. It will be appreciated that this further enhances the intubation device to provide additional functionalities whilst still leaving the other hand of the user free for other tasks.

In other improved embodiments of the intubation device having an auxiliary conduit, the auxiliary conduit may be used to enable different functionalities that do not necessarily involve the delivery of objects or fluids to the subject.

For example, another embodiment of an improved intubation device 1100 is shown in FIGS. 11A and 11C, in which the intubation device 1100 includes a fiber optic cable 1190 extending along its auxiliary conduit 1180. In this case, the intubation device 1100 includes a display unit 1160 for displaying images transmitted by the fiber optic cable 1190.

As per previous examples, the intubation device 1100 includes a laryngoscope blade 1110 having a tip 1111 and a base 1112, a handle 1120 attached to the base 1112 of the blade 1110 for allowing the intubation device 1100 to be held in a hand of a user, a channel for receiving an endotracheal tube 210, and a tube movement mechanism 1130 in the handle 1120 for moving the endotracheal tube 210 through the channel to thereby advance the endotracheal tube 210. The channel extends along the blade 1110 and partially along the handle 1120, the channel includes an outlet proximate to the tip 1111 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet, and the tube movement mechanism 1130 is configured to allow the user to hold the intubation device 1100 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

In this particular embodiment, the auxiliary conduit 1180 extends along the blade 1110 and the handle 1120, and includes an auxiliary outlet 1181 proximate to the tip 1111 for allowing a distal end 1191 of the fiber optic cable 1190 to collect light from a viewing area near the tip 1111, as in the configuration shown in FIG. 11A. The collected light will be transmitted along the fiber optic cable 1190 to the display unit 1160, which is configured to display an image on a display screen 1161 provided in a housing 1162 of the display unit 1160.

The display unit 1160 is connected to a cap 1150 that encloses the proximal end of the housing 1120. The fiber optic cable 1190 may be coupled to the display unit 1160 via the cap 1150. In this example, the fiber optic cable 1190 may be removed from the auxiliary conduit 1180 by removing the cap 1150 and the connected display unit 1160, as indicated in FIGS. 11B and 11C.

A similar configuration as shown in FIGS. 11A to 11C may be used to provide different functionalities via the auxiliary conduit 1180. For example, alternative forms of the delivery device 1100 may be provided where the auxiliary function includes causing an electrical signal to be transmitted via the auxiliary conduit 1180, such as via a wire or cable. For instance, the electrical signal may be in the form of a sensor signal received from a sensor, an actuator signal for activating an actuator, or a bioelectrical stimulus signal for transmission to a subject.

In any event, it will be appreciated that a diverse range of auxiliary functions may be provided using an auxiliary conduit provided in improved embodiments of single handed delivery devices as discussed above.

As mentioned in the previous examples, the improved embodiments of the intubation device may also include an auxiliary control for activating the auxiliary function. In some examples, the intubation device may include a first digit interface for allowing the user to operate the tube movement mechanism using a digit of the hand that is holding the intubation device, together with a second digit interface for allowing the user to activate the auxiliary function using a digit of the hand that is holding the intubation device.

So for the example delivery device 700 as shown in FIG. 7, the first digit interface may be a thumb interface of the tube movement mechanism 730, while the second digit interface may be provided in the form of a further finger or thumb operated interface which may be configured to activate an auxiliary movement mechanism for advancing the endoscope 790 through the auxiliary conduit 780. On the other hand, for the example delivery device 1001 as shown in FIG. 10A, the first digit interface may be a thumb interface of the tube movement mechanism 1030, and the second digit interface is the fluid delivery interface 1082 which causes delivery of a fluid through the auxiliary conduit 1080.

In any event, it will be appreciated that providing a second digit interface can allow both the main function of delivering the endotracheal tube and the auxiliary function to be provided using a single hand of the user, thereby leaving the user's other hand free for other tasks.

It should also be appreciated that a second digit interface can be provided for activating an auxiliary function in a range of different embodiments of intubation devices that do not necessarily involve the use of an auxiliary conduit as described in the above examples.

Accordingly, in some embodiments, the intubation device may broadly include the core elements of: a laryngoscope blade having a tip and a base; a handle attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a channel for receiving an endotracheal tube, the channel extending along the blade and partially along the handle, and the channel including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet; and a tube movement mechanism in the handle for moving the endotracheal tube through the channel to thereby advance the endotracheal tube, the tube movement mechanism being configured to allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand, and additionally include a first digit interface for allowing the user to operate the tube movement mechanism using a digit of the hand that is holding the intubation device, together with a second digit interface for allowing the user to activate an auxiliary function using a digit of the hand that is holding the intubation device.

Whilst an auxiliary conduit is not essential in all embodiments of intubation devices have such a second digit interface, it will be noted that many embodiments will have an auxiliary conduit for allowing an auxiliary function to be provided using the intubation device.

For instance, in embodiments where the auxiliary function includes causing an object to be delivered via the auxiliary conduit, the intubation device may include an auxiliary delivery mechanism for moving the object through the auxiliary conduit, and the second digit interface may thus be provided for activating the auxiliary delivery mechanism. Similarly, in embodiments where the auxiliary function includes causing a fluid to be delivered via the auxiliary conduit, the second digit interface may be provided for controlling the delivery of the fluid.

The second digit interface may also be employed in relation to other auxiliary functions, such as where the auxiliary function includes causing an electrical signal to be transmitted via the auxiliary conduit.

In another example, the auxiliary function may include causing the endotracheal tube to be disengaged from the tube movement mechanism, such that the second digit interface may be used to trigger this disengagement. For example, the tube movement mechanism may be configured so that clips (such as clips 633 in FIG. 6G), which are for engaging the endotracheal tube to retain the endotracheal tube and facilitate its movement, may be disengaged from the endotracheal tube in response to activation of the second digit interface, to thereby facilitate removal of the endotracheal tube from the delivery device.

Another particular example of an alternative auxiliary function that may be activated by a second digit interface is shown in FIG. 17. In this example, the intubation device 1700 includes a blade portion 1710, handle portion 1720 and tube movement mechanism 1740 which is operated using a first digit interface, and further includes a second digit interface in the form of a lever 1701 which may be used to activate a light 1740 provided on the blade portion 1710. The lever 1701 as shown in this example may be conveniently activated by one of the fingers of the user's hand when the intubation device 1700 is gripped in the same manner as shown in FIG. 3A.

In other alternative forms of an improved intubation device, the blade of the intubation device may include a moveable blade portion and the second digit interface may be provided for causing movement of the moveable blade portion. The moveable blade portion may be configured so that movement of the moveable blade portion varies at least one of: a position of the tip of the blade, an angle of at least a distal portion of the blade proximate to the tip, and a curvature of the blade.

An example of an intubation device 1800 including such a moveable blade portion is shown in FIGS. 18A and 18B and will now be described.

In this case, the intubation device 1800 includes a laryngoscope blade 1810 having a tip 1811 and a base 1812; a handle 1820 attached to the base 1812 of the blade 1810 for allowing the intubation device 1800 to be held in a hand of a user; a channel for receiving an endotracheal tube, the channel extending along the blade 1810 and partially along the handle 1820, and the channel including an outlet proximate to the tip 1811 for allowing a distal end of the endotracheal tube to be advanced from the outlet; and a tube movement mechanism 1830 in the handle 1820 for moving the endotracheal tube through the channel to thereby advance the endotracheal tube, the tube movement mechanism being configured to allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand. A first digit interface is provided for allowing the user to operate the tube movement mechanism 1530 using a digit of the hand that is holding the intubation device 1500, and a second digit interface is provided for allowing the user to cause movement of the moveable blade portion using a digit of the hand that is holding the intubation device 1500.

In this example, the second digit interface is again in the form of a lever 1801 that may be conveniently activated by the fourth digit of the user's hand when the intubation device 1800 is gripped in the same manner as shown in FIG. 3A. However, in this case, the level 1801 is configured to cause movement of the moveable blade portion.

In the current embodiment, the moveable blade portion is implemented by providing a series of articulated blade segments 1871, 1872, 1873 extending from the base 1812 of the blade 1810 and interconnected by pivot joints 1881, 1882, 1883, such that the blade segments 1871, 1872, 1873 may be articulated about the pivot joints 1881, 1882, 1883 under the control of the lever 1801.

For example, the blade segments 1871, 1872, 1873 may be coupled to the lever 1801 using a cable or the like, so that activation of the lever 1801 will effectively shorten the cable and cause the blade segments 1871, 1872, 1873 to articulate anteriorly relative to the subject as shown in FIG. 18B, which can be seen to have a smaller radius of curvature compared to FIG. 18A where the lever 1801 has not been activated.

In other words, the moveable blade portion and the second digit interface in this example are configured so that activation of the second digit interface causes the moveable blade portion to move so that the curvature of the blade is increased.

It will be appreciated that the moveable blade portion will include a corresponding portion of the channel that will effectively move along with the moveable blade portion.

The moveable blade portion may be specifically configured to vary the effective shape and/or the curvature of the blade 1810 as required to suit different subject anatomies or to allow fine tuning of the position and direction of the tip 1811 of the blade during an intubation procedure. This can be used to adjust the advancement path of the endotracheal tube during an endotracheal intubation procedure. The moveable blade portion can also be used to enhance the ability of the user to manipulate the tongue or other anatomical features of the subject during a procedure, without needing to mover the entire intubation device using the handle.

An intubation device having a moveable blade portion may facilitate manipulations of the tongue which may not otherwise be available using a fixed blade shape. In some implementations, this may open up the possibility of performing intubation on a sitting subject (as opposed to a supine subject), which may be desirable for some categories of subjects. When a subject is sitting, it can be difficult for a user to effectively manipulate the tongue using a fixed blade shape because this will require an unnatural upwards pulling action to be applied to the intubation device. However, an intubation device having a moveable blade portion may allow the required tongue manipulation without requiring the same upward pulling action.

It should be appreciated that the embodiment of FIGS. 18A and 18B is but one example of an implementation of a moveable blade portion, and a range of alternative implementations may be provided with similar overall functionalities.

In yet another example of an improved intubation device, the intubation device may include a moveable manipulator and the second digit interface may be provided for causing movement of the moveable manipulator. In such an example, the moveable manipulator may extend from one of: the tip of the blade; a distal portion of the blade proximate to the tip; and an intermediate portion of the blade between the tip and the handle.

In some examples, additional digit interfaces may be provided for enabling more than one auxiliary function, or for allowing different aspects of an auxiliary function to be controlled.

A specific example of an improved intubation device 1200 having a moveable manipulator will now be described with regard to FIGS. 12A and 12B.

The intubation device 1200 includes a laryngoscope blade 1210 having a tip 1211 and a base 1212, a handle 1220 attached to the base 1212 of the blade 1210 for allowing the intubation device 1200 to be held in a hand of a user, a channel for receiving an endotracheal tube 210, and a tube movement mechanism 1230 in the handle 1220 for moving the endotracheal tube 210 through the channel to thereby advance the endotracheal tube 210. The channel extends along the blade 1210 and partially along the handle 1220, the channel includes an outlet proximate to the tip 1211 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet, and the tube movement mechanism 1230 is configured to allow the user to hold the intubation device 1200 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

In addition, the intubation device 1200 includes a manipulator arrangement including: a moveable manipulator 1270 attached to the blade 1210, a manipulator actuator (not shown) for moving the manipulator 1270, and a manipulator control 1201, 1202 in the handle 1210. The manipulator control 1201, 1202 is configured to allow the user to operate the manipulator control 1201, 1202 using the same single hand.

It will be appreciated that, in this case, the intubation device 1200 includes a second digit interface and a third digit interface for providing two manipulator controls 1201, 1202.

In this example, the manipulator arrangement is configured to allow a manipulator tip 1271 of the moveable manipulator 1270 to be extended or retracted from the blade 1210, and thus a first manipulator control 1201 may be provided for allowing the user to control this extension/retraction.

This example of the manipulator arrangement is further configured to allow the manipulator tip 1271 to be repositioned in space, and thus a second manipulator control 1202 may be provided for allowing the user to control the position of the manipulator tip 1271 in opposing lateral directions and/or anteriorly/posteriorly relative to the blade 1210.

It will be appreciated that different embodiments of the intubation device 1200 may include only a subset of the above discussed manipulator movement capability and that the particular configurations of the manipulator actuator and manipulator controls may be adjusted accordingly to suit the particular moveable manipulator implementation.

It is also noted that the example of the intubation device 1200 in FIGS. 12A and 12B also includes a display unit 1260 connected to a cap 1250, where the display unit 1260 includes a display screen 1261 provided in a housing 1262, similar to the example of FIGS. 11A to 11C. In this case, the display unit 1260 allows visual feedback of the manipulator tip 1271 position to be provided to the user, so that the user can more effectively operate the manipulator controls to move the manipulator tip 1271 into a desired position with reference to images displayed on the display screen 1261 during the procedure.

A number of other optional improvements which may be applied to embodiments of the intubation devices as described above will now be discussed.

As discussed above with regard to the example of FIGS. 6A to 6G, embodiments of the intubation device may be used to intubate a patient while the patient is being supplied with oxygen via a mask that includes a suitably configured orifice for allowing insertion of the intubation device, without any interruption of the supply of oxygen to the patient during the intubation procedure. In this case, the intubation device may be provided with seals to thereby substantially prevent air from escaping from the mask via the intubation device.

A specific embodiment of an intubation device 1300 including examples of suitable seals in accordance with the above will now be described with regard to FIGS. 13A to 13C.

The intubation device 1300 includes a laryngoscope blade 1310 having a tip 1311 and a base 1312, a handle 1320 attached to the base 1312 of the blade 1310 for allowing the intubation device 1300 to be held in a hand of a user, a channel for receiving an endotracheal tube 210, and a tube movement mechanism 1330 in the handle 1320 for moving the endotracheal tube 210 through the channel to thereby advance the endotracheal tube 210. The channel extends along the blade 1310 and partially along the handle 1320, the channel includes an outlet proximate to the tip 1311 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet, and the tube movement mechanism 1330 is configured to allow the user to hold the intubation device 1300 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

In this case, the intubation device 1300 may be provided with seals 1301, 1302 across at least part of the channel and opening along the channel to thereby substantially prevent air from escaping from the mask via the intubation device 1300. In this example, a first seal 1301 is configured to snap onto channel portions adjacent to the channel opening as shown in FIG. 13A and is further configured to be removable to allow disengagement of the endotracheal tube 210 after successful intubation, as shown in FIG. 13C.

Furthermore, a second seal 1302 is provided in the form of a cuff seal configured to surround the endotracheal tube 210 within the blade channel portion 1313 as shown in the inset detail of FIG. 13B and thus prevent escape of air along the channel around the endotracheal tube 210. The second seal 1302 does not completely encircle the endotracheal tube 210, but instead includes a gap 1303 for allowing the endotracheal tube 210 to be removed from the second seal 1302 when it is disengaged from the intubation device 1300.

Another version of an intubation device 1300 including seals will now be described with regard to FIGS. 14A to 14C.

As per the previous example, the intubation device 1400 includes a laryngoscope blade 1410 having a tip 1411 and a base 1412, a handle 1420 attached to the base 1412 of the blade 1410 for allowing the intubation device 1400 to be held in a hand of a user, a channel for receiving an endotracheal tube 210, and a tube movement mechanism 1430 in the handle 1420 for moving the endotracheal tube 210 through the channel to thereby advance the endotracheal tube 210. The channel extends along the blade 1410 and partially along the handle 1420, the channel includes an outlet proximate to the tip 1411 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet, and the tube movement mechanism 1430 is configured to allow the user to hold the intubation device 1400 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

The intubation device 1400 is also provided with seals 1401, 1402 similar to those described for the previous example. These seals include a first seal 1401 configured to snap onto channel portions adjacent to the channel opening as shown in FIG. 14A and further configured to be removable to allow disengagement of the endotracheal tube 210 after successful intubation, as shown in FIG. 14C, together with a second seal 1402 in the form of a cuff seal having a gap 1403, where the second seal 1402 is configured to surround the endotracheal tube 210 within the blade channel portion 1413 as shown in the inset detail of FIG. 14B and thus prevent escape of air along the channel around the endotracheal tube 210.

In this specific example, the second seal 1402 is an inflatable balloon cuff seal and can be inflated or deflated as needed using an inflation syringe 1404 that is connected to the second seal 1402 using tubing 1405.

Some versions of the intubation device may be provided having an alternative configuration whereby the endotracheal tube is received inside an enclosed conduit. In these cases, the structural arrangement of the intubation device may need to be adapted to allow the endotracheal tube to be removed from the intubation device in different ways compared to previous examples, where it can simply be displaced from the opening of a channel.

In some embodiments, the intubation device may include a housing defining: a laryngoscope blade portion having a tip and a base; a handle portion attached to the base of the blade for allowing the intubation device to be held in a hand of a user; a conduit for receiving an endotracheal tube, the conduit extending along the blade portion and partially along the handle portion, and the conduit including an outlet proximate to the tip for allowing a distal end of the endotracheal tube to be advanced from the outlet; and a tube movement mechanism in the handle for moving the endotracheal tube through the conduit to thereby advance the endotracheal tube, the tube movement mechanism being configured to allow the user to hold the intubation device and advance the endotracheal tube in an endotracheal intubation procedure using a single hand.

In some particular versions, the housing may be configured to be split along the conduit to allow the endotracheal tube to be removed from the conduit. In other versions, the intubation device could be configured to otherwise allow the endotracheal tube to be removed via the distal end of the channel, noting that this may require the use of a non-standard endotracheal tube design.

In any event, a housing as discussed above may be provided using inexpensive materials such as plastic so as to be disposable, or on the other hand, it may be provided in a reusable form where the housing is capable of being sterilized for repeated usage.

A specific example of an intubation device 1500 having an enclosed conduit for receiving the endotracheal tube, as discussed above, will now be described with reference to FIGS. 15A and 15B.

In this case, the intubation device 1500 includes a housing defining: a laryngoscope blade portion 1510 having a tip 1511 and a base 1512; a handle portion 1520 attached to the base 1512 of the blade portion 1510 for allowing the intubation device 1500 to be held in a hand of a user; a conduit for receiving an endotracheal tube 210, the conduit extending along the blade portion 1510 and partially along the handle portion 1520, and the conduit including an outlet 1504 proximate to the tip 1511 for allowing a distal end of the endotracheal tube 210 to be advanced from the outlet 1504; and a tube movement mechanism 1530 in the handle 1520 for moving the endotracheal tube 210 through the conduit to thereby advance the endotracheal tube 210, the tube movement mechanism 1530 being configured to allow the user to hold the intubation device 1500 and advance the endotracheal tube 210 in an endotracheal intubation procedure using a single hand.

The housing is configured to be split along the conduit to allow the endotracheal tube 210 to be removed from the conduit. This is achieved by providing the housing in two separate housing parts 1501, 1502, which are joined along a seam 1503. Each housing part 1501, 1502 has a respective portion of the blade portion 1510 and the handle portion 1520, and can be split apart and separated laterally to allow the endotracheal tube 210 to be removed from the conduit after delivery.

The seam 1503 may be a single use frangible seam that can be broken when the housing parts 1501, 1502 are to be split apart, such that the intubation device would no longer be usable and thus would need to be disposed after use.

Alternatively, the seam 1503 may have a reusable configuration, such as by allowing a snap fit or clip style connection between the housing parts 1501, 1502 that can be repeatedly connected and disconnected as required.

It is noted this this example of the intubation device 1500 also includes a display unit 1560 connected to a cap 1550, similar to earlier examples. Whilst the housing parts 1501, 1502 may be provided in a disposable form, the display unit 1560 and the cap 1550 may be disconnected from the housing and reused many times.

Another embodiment of an intubation device 1600 is shown in FIG. 16, which includes a transparent portion 1601 of the blade portion 1610. Otherwise, the handle portion 1620 and other elements of the intubation device 1600 may be provided in accordance with previously described examples.

It will be appreciated that the shape of the different elements of the intubation device may also be varied without impacting on the above discussed functionality, such as to allow for more comfortable use. For example, FIGS. 19 and 20 show alternative embodiments of the intubation device having different handle shapes.

In FIG. 19, the intubation device 1900 has a straight handle 1920 which may provide for a grip and operation similar to that of a conventional laryngoscope. On the other hand, in FIG. 20, the intubation device 2000 has a posteriorly curved handle 2020 which can facilitate a different style of grip and also allow for a wider range of manipulation of the blade position without interfering with the subject's body.

It should be appreciated that the above described intubation device improvements may be incorporated with the previously developed examples of intubation devices, and more than one of the improvements may be incorporated in combination where these are compatible with one another. It should be appreciated that the different embodiments of the intubation devices may be modified to include one or more of the improvements as described above, in order to enable the described functionalities of the intubation device improvements.

It is noted that whilst the above examples of improvements refer to intubation devices that provide for single handed intubation, at least some of the above described improvements may be applied to other forms of intubation devices such as conventional laryngoscopes or variations thereof. Whether or not a particular improvement may be applied to non-single handed intubation device will become apparent to persons skilled in the art based on the context of the improvement and any dependence on functionalities particular to single handed intubation devices.

Throughout this specification and claims which follow, unless the context requires otherwise, the word “comprise”, and variations such as “comprises” or “comprising”, will be understood to imply the inclusion of a stated integer or group of integers or steps but not the exclusion of any other integer or group of integers. As used herein and unless otherwise stated, the term “approximately” means±20%.

It must be noted that, as used in the specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a support” includes a plurality of supports. In this specification and in the claims that follow, reference will be made to a number of terms that shall be defined to have the following meanings unless a contrary intention is apparent.

It will of course be realised that whilst the above has been given by way of an illustrative example of this invention, all such and other modifications and variations hereto, as would be apparent to persons skilled in the art, are deemed to fall within the broad scope and ambit of this invention as is herein set forth.

INTUBATION DEVICE IMPROVEMENTS

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