This invention relates to valves of the kind including an outer housing, a valve seat, a valve seal displaceable along the housing into or out of sealing engagement with the valve seat, a resilient member arranged to urge the seal into engagement with the seat and an actuator arrangement extending from the valve seal to an opening of the housing.
Various medico-surgical tubes, such as tracheal tubes, have an inflatable sealing cuff towards the patient end that can be inflated to seal the outside of the tube with a body cavity, such as the trachea. The cuff is inflated and deflated via a small bore lumen extending along the tube that connects towards its machine end with an inflation line terminated by an inflation indicator and a valve. The valve is arranged to remain closed, to block escape of air from the cuff, during use but can be opened by inserting the nose of a syringe or a similar inflation device into the valve to displace a valve element away from a valve seat and allow air to be supplied to or from the valve to inflate or deflate the sealing cuff. It is important that the valve work reliably so that air does not leak out from the cuff and so that it can be opened readily to allow the cuff to be deflated, such as when the tube needs to be removed. Usually, these valves include a spring element in the form of a helical metal wire to urge the valve element to the seated, closed position. One problem with valves including such a spring element is that they may not be compatible with MRI scanners. Although it is possible to use a non-metallic spring element, such as of a resilient plastics material, these can be difficult to manufacture reliably. In particular, thermoplastics can be susceptible to shrinkage after removal from the mould or as a result of sterilisation or ageing after storage. One form of valve is described in PCT/GB2016/000011.
Valves are also used in other applications in addition to sealing cuffs of medico-surgical tubes.
It is an object of the present invention to provide an alternative valve and a medico-surgical tube including such a valve.
According to the present invention there is provided a valve of the above-specified kind, characterised in that the actuator arrangement includes a latch member and is displaceable forwardly from an initial position before use where it is out of engagement with a latch surface on the housing to a second position where the latch member engages the latch surface and prevents movement of the actuator arrangement rearwardly beyond the latched position, that the actuator arrangement is displaceable forwardly from the latched position to displace the seal away from the seat and allow flow through the housing, and that the actuator arrangement, when released, allows the seal to be displaced by the action of the resilient member to return to engagement with the seat and prevent flow along the valve.
The latch member may include an outwardly displaceable spring element that is held inwardly in the initial position by engagement with an external surface formation and that moves resiliently outwardly when displaced forwardly to clear the surface formation, thereby enabling the spring element to engage the latch surface. The resilient member is preferably a non-metallic member, such as a ceramic and may be a helical spring. The valve may includes a cylindrical support member secured in the forward end of the outer housing, the support member having a rear projecting nose and an axial bore and the forward end of the helical spring embracing the rear projecting nose. Alternatively, the resilient member may be a cylindrical member of a plastics material.
According to another aspect of the present invention there is provided a medico-surgical tube including an inflatable sealing cuff encircling the tube, an inflation lumen extending along the tube and opening into the cuff at one end and a valve connected at the opposite end of the inflation lumen to allow or prevent gas flow to or from the cuff, the valve being a valve according to the above one aspect of the present invention.
The tube may be a tracheal tube.
A tracheal tube including a valve 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
With reference now also to
The support member 32 has an annular, projecting rib 33 midway along its length that engages and locates in the groove 29 to prevent movement along the housing 21. The support member 32 is typically bonded in the housing 21 by means of an adhesive, solvent or the like. At opposite ends, the support member 32 is formed with respective forward and rear projecting nose formations 34 and 35. A gas passage in the form of an axial bore 36 extends along the support member 32 and opens through the respective nose formations 34 and 35. The rearwardly-facing, right-hand nose formation 35 acts as a location to retain the forward end of a helical spring 40 that extends around the nose formation. The spring 40 has a circular section and extends along a helical path of circular section that extends axially of the housing 21. The spring 40 is made of an MRI-safe material, such as a non-magnetic and non-metallic material. Preferably, the spring 40 is of a ceramic material such as silicon nitride or a ceramic mixture including zirconia. Alternatively, the spring could be of a resilient polymer. The opposite, rear end of the spring 40 embraces a forwardly-facing nose formation 41 of the same shape as the nose formation 35 and formed at the forward end of an axially-displaceable valve member 42. The nose formation 41 projects centrally from a radial supporting disc 43 at the forward end of a valve stem 44. The valve member 42 supports a valve seal 45 in the form of an annular disc of a resilient, compliant material such as a soft, rubber-like material. The valve seal 45 embraces the valve stem 44 and its forward face lies against the rear face of the supporting disc 43. The opposite, rearwardly-facing surface of the valve seal 45 lies in contact with the valve seat provided by the forward surface of the ledge 28 around the opening 30 when the valve is in a closed state. The valve member 42 can be displaced forwardly against the resilience of the spring 40 to lift the seal 45 out of contact with the valve seat 28 and open the valve 20 in a manner described in more detail below.
The rear end of the stem 44 of the valve member 42 is slidably received in an axial cavity 50 (
The valve 20 is supplied to the user and is stored before use in the initial, inactivated position shown in
When the tracheostomy tube 1 is inserted in the patient and the cuff 10 needs to be inflated for the first time the user inserts the nose of a syringe into the luer bore 26 of the valve 20. The nose of the syringe displaces the actuator member 51 and the latch member 53 but initially does not displace the valve member 42 because of the separation between the rear end of the valve member stem 44 and the floor 51′ of the cavity 50. The latch member 53 moves forwardly until the rear end of the latching spring fingers 56 clear the forward end of the recess 60, thereby allowing the rear end of the spring fingers to snap outwardly to engage the latching surface 63 in the position shown in
To inflate the cuff 10 the syringe is pushed further into the valve 20 to a position where the outside of the nose of the syringe makes a luer slip fit with the bore 26. This displaces the actuator member 51 and valve member 42 together, thereby lifting the seal 45 off the valve seat 28 to open the valve and allow fluid, such as air or water to flow around the actuator member when the plunger of the syringe is depressed. Fluid flows through the opening 30, around the seal 45, through the turns of the spring 40 and along the bore 36 through the support member 32 and into the inflation indicator 14 attached to the forward end of the valve 20. From there, the fluid flows along the inflation line 13 and inflation lumen 12, out of the opening 11 and into the interior of the cuff 10. Fluid can also flow in the opposite direction.
Instead of using a helical spring to provide a resilient force urging the valve seal against a seat it would be possible to use other resilient means.
When the actuator member 151 is pushed forwardly, such as by the nose of a syringe, to open the valve, the valve member 86 is pushed forwardly to move the valve seal 87 forwardly away from the valve seat 128. This causes the resilient cylinder 80 to buckle slightly inwardly as it is compressed axially. Fluid can flow between the valve seal 87 and the seat 128 and between the inside of the housing 121 and the outside of the cylinder along the grooves 82 and through the slots to the inside of the cylinder so that it can then flow along the bore 134 through the support member.
The arrangement of the present invention enables a non-metallic, MRI-compatible resilient element to be used although the resilient element in the valve could be a conventional helical metal wire spring. The present invention provides a valve that can be latched into an operational position after an initial actuation. This arrangement allows for compensation of any dimensional change, especially shrinkage, of the plastic components of the valve that might take place over time such as after sterilisation or caused by ageing after prolonged storage. The valve components can be readily manufactured using conventional techniques, such as injection blow moulding. The invention accommodates variations in tolerances between components without affecting the performance of the valve, thereby enabling manufacturing costs to be kept to a minimum.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1515123.6 | Aug 2015 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/GB2016/000150 | 8/12/2016 | WO | 00 |