This invention relates to tracheostomy tube assemblies of the kind including a tracheostomy tube having a shaft with an inflatable sealing cuff towards its patient end and an inflation line communicating with the sealing cuff and having an inflation indicator towards its machine end.
Tracheal tubes are used to enable ventilation, respiration or spontaneous breathing of a patient. Endotracheal tubes are inserted via the mouth or nose so that one end locates in the trachea and the other end locates outside the patient. Tracheostomy tubes are inserted into the trachea via a surgically-formed opening in the neck. Tracheostomy tubes can be inserted by different techniques, such as the surgical cut-down procedure carried out in an operating theatre or a cricothyroidotomy procedure, which may be carried out in emergency situations.
Tracheostomy tubes are generally used for more long-term ventilation or where it is not possible to insert an airway through the mouth or nose. The patient is often conscious while breathing through a tracheostomy tube, which may be open to atmosphere or connected by tubing to some form of ventilator. The tube is secured in position by means of a flange fixed with the machine end of the tube and positioned to extend outwardly on opposite sides of the tube.
Tracheal tubes often have a sealing cuff on their outside close to the patient end. This usually takes the form of a cuff that is inflated by a gas or liquid so that, when inflated, it forms a seal with the tracheal wall, confining gas flow along the bore of the tube and preventing flow around its outside. The cuff is usually inflated and deflated by means of an inflation line in the form of a small-bore tube opening into the cuff at its patient end and extending along a channel along the outside of the shaft of the tube. The machine end of the inflation line extends freely beyond the channel and is terminated by a combined inflation indicator, connector and valve. Alternatively, the tracheal tube may have an inflation lumen extending within the wall of the shaft of the tube and joined towards the machine end of the shaft with a separate small-bore inflation tube. The nose of a syringe or the like is inserted in the connector, opening the valve so that inflation gas or liquid can be supplied to or from the sealing cuff via the inflation line. The inflation indicator usually takes the form of a small flexible envelope or balloon connected at one end with the connector. The inflation line extends and opens into the interior of the inflation indicator so that the indicator is inflated by pressure in the sealing cuff and inflation line. If the pressure in the sealing cuff should fall this would be indicated by a corresponding deflation of the inflation indicator.
A problem occurs when tracheostomy tubes with such indicators are used with children. The soft nature of the inflation indicator and the proximity of the inflation indicator to the child's mouth means that the indicator can be easily chewed or bitten. This is a problem because, if the indicator or inflation line should be damaged, it may permit the inflation gas or liquid to escape thereby allowing the sealing cuff to deflate. This could allow ventilation gas to pass around the outside of the tracheostomy tube and prevent correct ventilation of the patient. The child chewing the inflation line and indicator may also ingest a part of the indicator.
It is an object of the present invention to provide an alternative tracheostomy tube assembly.
According to one aspect of the present invention there is provided a tracheostomy tube assembly of the above-specified kind, characterised in that the assembly also includes a protective enclosure extending around and enclosing the inflation indicator to protect it from damage by chewing, and that the protective enclosure is transparent, at least in part, to enable the inflation indicator to be viewed through the enclosure.
The protective enclosure preferably has a first part arranged to receive a machine end of the inflation indicator and a second part having a transparent sleeve adapted to extend around the inflation indicator and fit with the first part. The second part is preferably open at its machine end that fits with the first part, and the second part preferably has an opening at its patient end through which the inflation line extends and has a slot extending along its length between the open machine end and the opening at the patient end so that the inflation line can be threaded through the slot. The second part may have a projecting rim at one end adapted to engage a groove around the first part. The inflation indicator preferably has a substantially flat inflatable balloon, the protective enclosure including two opposite slots aligned with opposite edges of the balloon. The protective enclosure may include at least one projecting feature adapted to be chewed by the patient. The at least one projecting feature may be provided by two flanges oriented with the planes of the flanges substantially orthogonal to one another.
According to another aspect of the present invention there is provided a protector for an inflation indicator of a tracheostomy tube, characterised in that the protector is adapted to extend around and enclose the inflation indicator to protect it from damage by chewing, and that the protector is transparent, at least in part, to enable the inflation indicator to be viewed through it.
The protector may have a first part arranged to receive the machine end of the inflation indicator and a second part having a transparent sleeve adapted to extend around the inflation indicator and fit with the first part. The sleeve may be open at its machine end that fits with the first part, and the sleeve may have an opening at its patient end through which the inflation line extends and have a slot extending along its length between the open machine end and the opening at the patient end so that the inflation line can be threaded through the slot.
According to a further aspect of the present invention there is provided a tracheostomy tube assembly including a tracheostomy tube having an inflatable sealing cuff towards its patient end and an inflation line terminated by an inflation indicator at its machine end, characterised in that the assembly includes a protector for the inflation indicator according to the above other aspect of the present invention.
According to a fourth aspect of the present invention there is provided a method of forming a paediatric tracheostomy tube assembly including the steps of providing a paediatric tracheostomy tube with a sealing cuff and an inflation indicator, providing a protective enclosure in two parts comprising a base part and a transparent sleeve, fitting the sleeve over an inflatable part of the inflation indicator, and joining one end of the sleeve to the base part such that the machine end of the inflation indicator is received in the base part.
The transparent sleeve preferably has a slot extending longitudinally of the sleeve between openings at opposite ends of the sleeve such that the inflation line can be threaded sideways through the slot and then the sleeve can be slid along the inflation line to enclose the inflation indicator.
According to a fifth aspect of the present invention there is provided a paediatric tracheostomy tube assembly of a tracheostomy tube and a protector formed by a method according to the above fourth aspect of the present invention.
A paediatric tracheostomy tube assembly with an inflation indicator and protector, both according to the present invention will now be described, by way of example, with reference to the accompanying drawings in which:
With reference first to
The machine end 14 of the shaft 10 is adapted, during use, to be located externally of the tracheostomy opening formed in the patient's neck. The machine end 14 of the shaft 10 is bonded into a hub or connector 15 having a conventional 15 mm male tapered outer surface 16. The connector 15 is adapted to make a removable push fit in a conventional 15 mm female connector (not shown) at one end of a breathing tube extending to a ventilator or anaesthetic machine. Alternatively, the machine end of the tube 1 could be left open to atmosphere when the patient is breathing spontaneously. The tracheostomy tube 1 also includes a radially-extending support flange 20 adapted to lie against the skin surface of the neck on either side of the tracheostomy stoma. The flange 20 is moulded integrally as one part with the shaft 10 at its machine end 14 or may be formed separately. The flange 20 has openings 21 at opposite ends for attachment to a neck strap (not shown) used to support the tube with the patient's neck.
The shaft 10 also includes an inflation line 31 in the form of a small-bore tube secured in a channel 32 extending along the outside of one side of the shaft. The inflation line 31 has an opening 33 towards its patient end located approximately midway along the length of the sealing cuff 13. The machine end of the inflation line 31 extends through the flange 20 and continues unattached with the shaft 10 being joined with and extending into one end 36 a conventional inflation indicator 37. The inflation indicator 37 includes a flat, flexible envelope or balloon 38 into which the inflation line 31 opens so that the balloon is inflated or deflated according to the inflation state of the sealing cuff 13. The opposite end of the inflation indicator balloon 38 is bonded to one end of the outside of a rigid connector sleeve 39 containing a valve (not visible in the drawing) and being open at its machine end 40 to receive a male coupling such as the nose of an inflation syringe.
As so far described the tracheostomy tube assembly is conventional. The assembly differs from conventional tracheostomy tubes by the addition of a protector enclosure 50 adapted to extend around and enclose the inflation indicator 37 to protect it from damage by chewing.
The protector enclosure 50 is completed by a second part 60 in the form of a transparent cylindrical sleeve. The sleeve 60 is moulded of a stiff, transparent plastics material and is circular in section with an open machine end 62 having an outwardly projecting annular rim 63 the external diameter of which is such that it snaps into an internal retaining groove (not shown) around the inside of the base 51. The patient end 64 of the sleeve 60 is closed apart from a small opening 65 just large enough to receive the inflation line 31. The sleeve 60 also has two diametrically opposite slots 66 and 67 extending longitudinally of the sleeve. One slot 66 opens at its machine end into the open machine end 62 of the sleeve 60 and opens at its opposite end into the small patient-end opening 65 of the sleeve. The other slot 67 is shorter and terminates before the machine end opening 62 and the patient end opening 65. The longer slot 66 enables the sleeve 60 to be slid onto the inflation line 31 sideways and also gives the sleeve some resilience so that it can be squeezed to reduce the diameter at its machine end 62 and enable this to be inserted into the patient end of the base 51. The sleeve 60 also has two locking features 68 and 69 on opposite sides of its outer surface, midway between the two slots 66 and 67 and about half way along the length of the sleeve. The locking features 68 and 69 are shaped to clip onto the two notches 56 and 57 on outside of the base 51. Engagement of the locking features 68 and 69 on the sleeve 60 with the notches 56 and 57 on the base 51 prevents the sleeve rotating relative to the base.
The protective enclosure 50 could be permanently fitted onto the inflation indicator 37 by applying a bonding agent to the machine end of the sleeve 60 so that it becomes securely and permanently bonded to the base part 51. Alternatively, the sleeve 61 need not be bonded to the base 51 so that the protector 50 can be removed from the inflation indicator 37 when necessary.
The protector enclosure 50 is fitted on the inflation indicator 37 by first sliding the inflation line 31 sideways through the long slot 66 of the sleeve 61 at a location spaced a short distance away from the inflation balloon. The sleeve 61 is then oriented so that the opposite slots 66 and 67 align with the edges of the inflation balloon 38. The sleeve 61 can then be threaded rearwardly along the inflation line 31 and along the outside of the inflation indicator 37 as far as it will go. The assembly of the inflation indicator 37 and sleeve 61 is then slid rearwardly into the patient end of the base 51, aligning the locking features 68 and 69 on the sleeve with the notches on the base. The sleeve 61 is squeezed at the same time to compress the slots 66 and 67 so as to enable the rim 63 to enter the base 51 and then open into the internal retaining groove when released. Instead of loading the sleeve 61 onto the inflation indicator 37 first it would be possible to insert the inflation indicator into the base first and then slide the sleeve over and along the inflation indicator into the base.
With the inflation indicator 37 contained within the protective enclosure 50 the balloon 38 can inflate and deflate in the usual manner and the state of inflation of the indicator can be viewed through the transparent sleeve 60. If the child patient should chew on the assembly, the inflation indicator 37 will not be damaged because it is protected by the protector 50.
The protector 50 can be readily fitted to a conventional inflation indicator of a tracheostomy tube without the need for any special tools. The protector could be provided separately of the tracheostomy tube and assembled on the inflation indicator by the user, if needed. The protector need not be fitted by a clinical specialist but can be fitted by a child's carer at home as needed.
The protector could be provided with features specifically designed for the patient to chew so that he does not chew other parts of the protector. One example of a protector 150 with such features is shown in
Number | Date | Country | Kind |
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1907094.5 | May 2019 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/GB2020/000056 | 4/23/2020 | WO | 00 |