GB2341101A

GB2341101A - A breathing indicator device

Info

Publication number: GB2341101A
Application number: GB9919546A
Authority: GB
Inventors: Eric Pagan
Original assignee: Smiths Group PLC
Current assignee: Smiths Group PLC
Priority date: 1998-09-02
Filing date: 1999-08-19
Publication date: 2000-03-08
Anticipated expiration: 2019-08-19
Also published as: DE19940160A1; US6378522B1; JP2000070371A; FR2782646A1; JP4177938B2; GB2341101B; DE19940160B4; GB9919546D0; FR2782646B1; GB9819089D0

Abstract

An indicator 3 for a respiration device, preferably an endotracheal tube, to detect patient breathing is disclosed. One end 20 of a housing 2, preferably a transparent plastic connector, is adapted to connect to a respiration device and an indicator assembly is detachably secured in the opposite machine end 22. Preferably the indicator assembly is a frame 30, supporting an indicator element 31 extending within a lumen of the housing. The indicator element may be paper including a carbon dioxide colour change indicator chemical. Preferably a handle 39 on the frame 30 extends along the outside of the housing 2 so that the indicator 3 can be removed. Whilst the indicator 3 is fitted it prevents another connector from being attached to the housing 2.

Description

2341101 RESPIRATION ASSEMBLIES AND INDICATORS This invention relates to

respiration assemblies and to indicators.

The invention is more particularly concerned with assemblies with provision for detecting correct placement of an endotracheal tube or for indicating patient breathing.

One of the major problems associated with the use of an endotracheal tube is that of ensuring that the patient end of the tube is correctly located in the trachea and not in the oesophagus. There are various ways in which correct intubation can be detected. The usual way is to connect the machine end of the tube to a capnograph, which is responsive to the levels of carbon dioxide. When the tube is correctly inserted, the level of carbon dioxide detected will rise and fall with the patient's breathing. By detecting this alternating level of carbon dioxide, correct intubation is indicated. If the tube is incorrectly inserted, in the oesophagus, any carbon dioxide produced by the digestive system will be at a relatively steady level. Capnographs can produce a reliable indication of correct intubation but the equipment is relatively bulky and expensive so it is only available in well-equipped surgical operating theatres.

An alternative device can be used to detect carbon dioxide, which includes a chemical colour-change indicator, such as described in, for example, W096/24054, EP509998, US5005572, US4879999, EP257916, US4691701, US4790327, W089/07956, GB2218515 and US4728499. This form of device usually comprises a paper or some other substrate that 2 is impregnated or coated with the chemical including a pH-sensitive indicator dye, the substrate preferably being provided in some form of transparent connector attached to the machine end of the tube. Such indicators can be of low cost and can provide a clear indication that the tube has been correctly inserted. If the indicator fails to change colour, the clinician knows immediately that the tube has been incorrectly inserted. These prior indicators are designed to be left in position on the connector during use of the tube. This can, however, be a disadvantage because, to be effective, the indicator must be exposed to the maximum gas flow, thereby inevitably providing some impediment to gas flow. Also, where the indicator is positioned in the main gas flow path, this may prevent access to the tube, such as by a suction catheter or the like.

It is also useful in some circumstances to have a readily visible indicator confirming that the patient is breathing on other respiration devices, such as face masks or the like.

It is an object of the present invention to provide an improved respiration assembly and indicator.

According to one aspect of the present invention there is provided a respiration assembly including a respiration device, a housing mounted with the respiration device and an indicator assembly mounted in the housing, the indicator assembly having an indicator element mounted to extend within a lumen through the housing, and the indicator assembly being detachably secured in the housing such that the indicator assembly can be removed from the machine end of the housing.

3 The housing is preferably of a transparent plastics material and is preferably a connector. Ile indicator assembly is preferably shaped to prevent the connector mating with another connector while the indicator assembly is secured with the connector. The indicator assembly may be a push fit in the machine end of the housing. The indicator assembly preferably comprises a frame and an indicator element supported on the frame. The frame may comprise a circular ring attached coaxially with one end of the housing and a projecting member extending substantially axially of the housing, the indicator element being supported on the projecting member. The indicator element is preferably of a paper including a carbondioxide colour-change indicator chemical. The indicator assembly preferably includes a handle extending along the outside of the housing by which the indicator assembly can be gripped to remove it from the housing. The respiration device may be an endotracheal tube.

According to another aspect of the present invention there is provided an indicator for indicating patient breathing, the indicator having an outer housing adapted for connection at one end to a respiration device and an indicator assembly detachably secured in the housing and removable from the opposite end of the housing.

According to a fiirther aspect of the present invention there is provided a method of determining correct intubation of a patient comprising the steps of introducing into the trachea of the patient an endotracheal tube assembly of the End including an endotracheal 4 tube, a connector mounted at the patient end of the tube and an indicator assembly mounted in the connector, observing the indicator assembly to ensure correct intubation, and 4 subsequently removing the indicator assembly from the connector while leaving the connector in position on the tube.

An endotracheal tube assembly and its method of use, in accordance with the present invention, will now be described, by way of example, in which:

Figure 1 is a side elevation view of the assembly; Figure 2 is a perspective view of a part of the assembly to a larger scale; Figure 3 is a sectional side elevation view of the part shown in Figure 2; Figure 4 is an exploded, perspective view of the part shown in Figures 2 and 3; Figure 5 is a perspective view of an alternative part of the assembly; and Figure 6 illustrates steps in the use of the assembly.

With reference first to Figure 1, the assembly comprises an endotracheal tube 1, a connector 2 mounted in the machine end of the tube, and an indicator assembly 3 mounted in the connector.

The endotracheal tube I is of conventional construction, comprising a curved tubular shaft 10 with an inflatable cuff 11 encircling the shaft close to the open, patient end 12. The machine end 14 of the tube I is also open and is securely connected to the connector 2, which is shown in more detail in Figures 2 to 4, and takes the form of a breathing indicator.

The connector 2 is moulded from a rigid, transparent plastics material and has a tapered forward end 20 of relatively small diameter, which is a push fit within the machine end 14 of the tube I and may be bonded to it by means of a solvent or adhesive. Midway along its length, the connector has a radially-projecting flange 2 1, which divides the forward end 20 from the rear or machine end 22. The rear end 22 is enlarged with an external diameter of 15mm and a shallow luer taper adapted to receive a cooperating female tapered connector. The interior of the forward and rear ends 20 and 22 communicate with one another, forming a bore or lumen 24 through the connector.

The indicator assembly 3 comprises a moulded plastic support fi=e 30 and an indicator element 31 retained on the frame. The fi-ame 30 has an outer, circular ring 32, which, in section is of angled shape, having a horizontal portion 33, which sits coaxially on the end of the rear end 22 of the connector 2 providing a housing for the assembly 3. The frame 30 has a vertical portion 34, which is a tight fit within the rear end of the connector and may have barbs or fins to improve the grip on the inside of the connector 2. The fi-ame 30 also has a lateral bar 36 extending diametrically across the ring 32, the central part of the bar being bent down or forwardly into a V-shape formation 37, projecting axially of the connector 2. The underside of the bar 36 has two fixing lugs 38 with arrow-shape heads projecting down 6 on opposite sides of the V-shape formation 37. The fi-ame 30 also has a lever 39 of rectangular shape attached with the outside of the ring 32 by two reduced thickness hinge portions 40. The lever 39 normally extends down or forwardly along the outside of the rear part 22 of the connector 2.

The indicator assembly 3 is completed by the indicator element 3 1. The indicator element 31 is a strip of paper into which is absorbed a conventional carbon dioxide colourchange indicator chemical, which may be of the kind described in any of the patents referred to in the introduction. The indicator strip 31 is bent to form a central V-shape portion 40 conforming to the shape of the V-shape formation 37 on the frame 30. The ends 41 of the strip 31 extend horizontally outwardly and have fixing holes 42 shaped and positioned to receive the heads of the fixing lugs 38. The strip 31 is mounted underneath the lateral bar 36, with the V-shape portion 40 extending around the V-shape formation 37 on the bar 36 and with the ends 41 being retained by the fixing lugs 38. The indicator strip 31 extends across the lumen 24 of the connector 2, with the lower, central portion 40 projecting down within the connector along a major part of the length of its rear end 22. The dimensions of the indicator assembly 3 and the indicator strip 31 are such that the strip is clearly visible through the wall of the connector 2, whilst allowing air to flow along the lumen 24 of the connector.

Me indicator assembly 3 is removable from the rear end of the connector 2, as shown in Figure 4, by gripping the lower end of the lever 39, lifting this up so that it hinges about the hinge portions 40, and then pulling the indicator by the lever rearwardly out of the connector.

7 1. ' There are various other ways in which a similar indicator assembly could be attached to a connector instead of by the push, friction fit described above. For example, the indicator assembly and connector could be threaded so that the indicator assembly is removed by unscrewing. Alternatively, the indicator assembly and connector could have cooperating surface formations that snap fit together. In other arrangements, the indicator assembly could be attached with the connector by a tear seal, or by a spot or tack weld. A flirther arrangement is shown in Figure 5 where the indicator assembly 3' has a hinged or flexible clip 39' that fastens over a lug 2Pprojecting outwardly of the connector T.

In use, the assembly is supplied with the connector 2 and indicator assembly 3 ready fitted in the machine end 14 of the tube 1, so that the clinician can readily insert the tube into the patient without the need for further assembly. If the tube 1 is correctly inserted with its. patient end 12 located in the trachea, the indicator assembly 3 will be exposed to the patient's inhaled and exhaled breath flowing along the tube. Because the exhaled breath contains a relatively high concentration of carbon dioxide, this causes the indicator strip 31 to change colour during exhalation. When the patient inhales, the colour of the strip 31 changes back towards its normal colour. In this way, the colour of the indicator strip 31 alternates with the patierifs breathing. The clinician observes the indicator assembly 3 and, when this confirms correct intubation, he inflates the cuff 11 to seal the tube 1 with the trachea and to retain it in position. He then removes the indicator assembly 3 by pulling it out of the connector 2 in the 1 way described above, and as shown in Figure 6, so as to maximize the passage through the connector and enable access by a suction catheter or the like should this be necessary. If the patient is breathing spontaneously, the connector 2 may be left open. If assisted ventilation is needed, the connector 2 can be connected to a cooperating male connector 50 connected to ventilation tubing 51 extending to ventilation equipment (not shown). If the indicator assembly 3 were left in place, itwould prevent connection by the ventilation connector 50; this ensures that the indicator assembly is removed before connection.

The invention could be used with other respiration devices than endotracheal tubes. For example, an indicator according to the invention could be provided on a face mask to indicate patient breathing.

9

Claims

A respiration assembly including a respiration device, a housing mounted with the respiration device and an indicator assembly mounted in said housing, wherein said indicator assembly has an indicator element mounted to extend within a lumen through said housing, and wherein the indicator assembly is detachably secured in said housing such that said indicator assembly can be removed from the machine end of said housing.
2. An assembly according to Claim 1, wherein said housing is of a transparent plastics material.
3. An assembly according to Claim I or 2, wherein said housing is a connector.
4. An assembly according to Claim 3, wherein said indicator assembly is shaped to prevent said connector mating with another connector while the indicator assembly is secured with the connector.
5. An assembly according to any one of the preceding claims, wherein the indicator assembly is a push fit in the machine end of the housing.
6. An assembly according to any one of the preceding claims, wherein the indicator assembly comprises a frame and an indicator element supported on the frame.
7. An assembly according to Claim 6, wherein the fi-ame comprises a circular ring attached coaxially with one end of said housing and a projecting member extending substantially axially of the housing, and wherein said indicator element is supported on said projecting member.
8. An assembly according to Claim 6 or 7, wherein said indicator element is of a paper including a carbon dioxide colour-change indicator chemical.
9. An assembly according to any one of the preceding claims, wherein the indicator assembly includes a handle extending along the outside of the housing by which the indicator assembly can be gripped to remove it from the housing.
10. An assembly according to any one of the preceding claims, wherein the respiration device is an endotracheal tube.
11. An indicator for indicating patient breathing, wherein the indicator has an outer housing adapted for connection at one end to a respiration device and an indicator assembly detachably secured in said housing and removable from the opposite end of the housing.
12. A method of determining correct intubation of a patient comprising the steps of introducing into the trachea of the patient an endotracheal tube assembly of the kind including an endotracheal tube, a connector mounted at the patient end of the tube and an indicator assembly mounted in said connector, observing said indicator assembly to ensure correct intubation, and subsequently removing said indicator assembly from said connector while leaving said connector in position on said tube.
13. An endotracheal tube assembly substantially as hereinbefore described with reference to Figures 1 to 4 and Figure 6 of the accompanying drawings.
14. An endotracheal tube assembly substantially as hereinbefore described with reference to Figures 1 to 4 and Figure 6, as modified by Figure 5 of the accompanying drawings.
15. Any novel and inventive feature or combination of features as hereinbefore described.