THIS INVENTION relates to a respiratory or breathing circuit, more specifically to a paediatric anaesthesia circuit.
Paediatric care often requires specialist carers and equipment, to deal with the wide variety of conditions that may affect babies, children and young people. In some cases, anaesthesia circuits intended for adult use are used in paediatric care. Sometimes, paediatric circuits are simply smaller than their adult equivalents, but additional features may also be included for added safety or convenience. Use of circuits intended for adults in paediatric care can be inconvenient in some cases, but ineffective or even dangerous in others.
An improved circuit system is sought to provide a cost-effective but more versatile and safer system suitable for paediatric anaesthesia care.
The inspiratory tube 201 and expiratory tube 203 are suitable for connecting to a ventilator 110 (not shown) to aid respiration of the patient. The angle piece connector 202 connects to the patient via a mask or a tracheal or intubation tube (not shown). The circle system 200 may optionally further comprise a (closed) reservoir bag (not shown), e.g. for induction of anaesthesia.
Most ventilators/anaesthesia delivery units have at least three ports:
If the anaesthetist chooses to use the circle system only with its reservoir bag for induction of anaesthesia and then followed by automatic ventilation, then this is possible without using the T-piece system. Alternatively, the anaesthetist can use the T-piece system for induction followed by the circle system—here they have to ensure that they switch between the two breathing circuits appropriately.
‘Paediatric Anaesthesia for beginners’ (Dr. Tom Lawson, 2011), available online at: http://www.apagbi.org.uk/sites/default/files/images/APA%20Guide%20latest%20Version%2011_9_13.pdf sets out additional background to the present invention. Protection may be sought for features disclosed in the present application in combination with material known in the art, including this referenced material.
For paediatric care, the best systems are designed specifically for paediatric use, e.g. by being suitably sized, lightweight and with the T-piece having an appropriately-sized reservoir bag, e.g. half a litre.
The inventors have designed a paediatric anaesthesia circuit operable in multiple modes with a mechanism for safely switching therebetween. The claimed invention is beneficial because it provides a relatively simple, efficient system that reduces storage space, material use and manufacturing costs whilst greatly enhancing convenience for the anaesthetist and safety for the patient.
A first aspect of the present invention provides a breathing circuit for delivering a flow of gases to a patient, comprising:
The present invention further provides a breathing circuit as claimed.
In order for the present invention to be more readily understood, prior art and preferable embodiments of the invention are described, by way of example only, with reference to the accompanying drawings, in which:
a and 10b are perspective schematics of a second valve system for the present invention;
The system 1 further comprises a flow switch in the form of a valve 5 (better shown in
In essence, comparing the embodiment of
The switch/valve 5 of the circuit 1 and its operation are now described in more detail. Preferred embodiments are described in relation to the breathing circuit 1, but protection may be sought for the switch/valve 5 in isolation.
One embodiment of the valve 5 is shown in detail in
The circuit 1 is shown connected to a ventilator 10 in
In some embodiments, the circle flow portion of the circuit 1 additionally comprises a closed reservoir bag at a T-junction along the first expiratory tube 8, wherein the first expiratory tube 8 passes flow back to the ventilator past the closed reservoir bag. One-way flow valves may also be provided to direct flow appropriately through the circuit 1.
The system 1 of
In this embodiment, the valve 5 is controlled by manual rotation and
In this embodiment, the valve profile is generally L-shaped.
The switch 5 is constructed from a rigid/hard material and the preferred diameter of the tubes that attach at points A, B, C and D are 10 mm for the tubes in the T-piece system and 15 mm for the tubes in the circuit system.
A preferred second embodiment of the valve 5 is illustrated in
Preferably, the valve plungers are colour-coded to aid the operator in switching between circuits.
In some embodiments, the valve 5 is biased using a biasing element 13, e.g. a spring, preferably biased into one flow path/mode, so that the operator must keep the plunger depressed to permit flow into other flow paths/modes. A locking mechanism may be provided for securing the valve against the biasing element. In some embodiments, the biasing is to the first expiratory flow path which returns to the ventilator 10, since the reservoir bag 9 circuit is normally used for shorter periods. In other embodiments, the biasing is to the second expiratory flow path, using the T-piece system.
In other embodiments, biasing elements such as springs are provided on both sides of the valve 5 to bias the valve 5 out of both T-piece and circle flow modes and into a third mode, which may be a ‘no-flow’ mode where both expiratory flow paths are closed and the operator must operate the valve 5 to use either other flow mode. This additional ‘no flow’ mode acts as a safety mechanism to ensure the operator selects a suitable flow mode.
In the embodiment of
The locking mechanism comprises a notch or groove in an inner portion of a housing of the valve system and a tongue attached to the plunger, wherein the tongue is received in the notch, against the biasing force of the biasing element 13 to secure the valve 5 in the ‘active’ or locked position. In the embodiment shown, the tongue is rotated relative to the housing to engage the groove. O-rings 14 are provided to seal each expiratory flow path when not in use and the inner parts of the housing adjacent to the opening between the first and second expiratory tube 7,8 taper towards the opening, provide increased pressure at the periphery of the flow path, thus providing an improved seal. In this embodiment, the valve 5 is manually operated, but in other embodiments the valve may be electronically operated.
This third embodiment of the valve 5 is beneficial over the earlier embodiments because it is more compact, requires a single biasing element 13 in the form of a spring, and includes a locking mechanism to permit flow of anaesthetic gases and oxygen ONLY via the circle system. The valve 5 is also a single action switch rather than a shuttle valve, giving fewer points of possible failure.
In preferred embodiments, the circuit 1 further comprises a visual or audible indicator, such as a display or a light, for indicating a status of the circuit 1, e.g. OFF, STANDBY (system on but not in use) and the (expiratory) flow path (i.e. the flow mode e.g.: NO FLOW, RETURN/CIRCLE, FRESH FLOW/T-PIECE) in use. In further preferred embodiments, the circuit 1 further comprises a communications module for transmitting data preferably including the flow mode or flow parameters to other components and/or external devices (those not forming part of the breathing circuit itself), such as the ventilator 10.
Switching between separate T-piece and circle systems generally necessitates changes in the ventilator mode (from return flow to non-return/fresh flow and vice versa) and the present invention can eliminate the risk associated therewith by combining the two systems to avoid the need to switch the mode or automatically changing the mode of the circuit/ventilator where necessary, as appropriate. In further preferred embodiments, the circuit 1 is configured to switch a flow mode or parameter of the ventilator 10 and/or of the circuit 1 to coincide with the other of the ventilator 10 and the breathing circuit 1, to ensure that the two systems (the breathing circuit 1 and the ventilator 10) are configured to work together correctly. This is advantageous as it can prevent inappropriate use of the wrong circuit/wrong ventilator mode or unsuitable flow parameters.
For example, when the circuit is in the first flow mode to/from the ventilator, the circuit 1 communicates with the ventilator 10 and confirms that the ventilator 10 is functioning in the appropriate (return) flow mode with suitable flow parameters, else the system may be configured to switch a predetermined one of the circuit 1 and the ventilator 10 so that the modes coincide and/or the flow parameters are suitable, or to disable all flow and sound an alarm or display a message on a display. For example, ventilator or breathing circuit 1 may comprise a storage medium that stores acceptable or non-acceptable combinations of flow modes and/or flow parameters and the system checks the initial settings against the acceptable or non-acceptable combinations before making an adjustment or notifying the user.
The circuit 1 may therefore comprise a processor, sensor(s), motor(s), memory and/or a communications module configured to sense a position of the valve 5 and therefore determine the flow mode, and then communicate the mode to other components of the system or external devices such as the ventilator 10, preferably adjusting the flow mode of the circuit 1 in response to sensed information or data received from the external devices, or sending configuration information to adjust the component/external device for compatibility with the circuit 1. Particularly suitable sensors include temperature sensors, humidity sensors and flow rate sensors.
Preferably, the external device (ventilator 10) or the breathing circuit 1 can be configured as a MASTER device, with the other of the external device (ventilator 10) and the breathing circuit 1 thereby being configured as a SLAVE device and the slave device adjusts to function correctly with the master device.
In some embodiments, the circuit 1 comprises the ventilator 10, which may be an anaesthesia ventilator configured to deliver aesthetic gases to the patient.
Preferably, the ventilator comprises a communications module and the ventilator is configured to:
When used in this specification and claims, the terms “comprises” and “comprising” and variations thereof mean that the specified features, steps or integers are included. The terms are not to be interpreted to exclude the presence of other features, steps or components.
The features disclosed in the foregoing description, or the following claims, or the accompanying drawings, expressed in their specific forms or in terms of a means for performing the disclosed function, or a method or process for attaining the disclosed result, as appropriate, may, separately, or in any combination of such features, be utilised for realising the invention in diverse forms thereof. In particular, any specific element of one or more embodiments may be combined with any other embodiments disclosed herein.
Number | Date | Country | Kind |
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1607682.0 | May 2016 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/GB2017/051235 | 5/3/2017 | WO | 00 |