Title:
VENTILATORS
United States Patent 3768468


Abstract:
A lung ventilator in which the volume of respirable gas passing to the patient per unit time is continuously measured and the flow stopped, to mark the end of the inspiratory phase and the start of the expiratory phase, when a chosen volume has passed through the meter.



Inventors:
COX L
Application Number:
05/106960
Publication Date:
10/30/1973
Filing Date:
01/18/1971
Assignee:
BRITISH OXYGEN CO LTD,GB
Primary Class:
Other Classes:
137/908
International Classes:
A61B5/091; A61M16/00; (IPC1-7): A61M16/00
Field of Search:
128/145
View Patent Images:
US Patent References:
3633576VOLUMETRIC RESPIRATORJanuary 1972Gorsuch
3628042CONTROL SYSTEMDecember 1971Jacobus
3530872RESPIRATORY APPARATUSSeptember 1970Arp
3523527ELECTRONICALLY CONTROLLED VARIABLE MODE RESPIRATORAugust 1970Foster
3357428Respiratory augmentor with electronic monitor and controlDecember 1967Carlson
3191595Electrically controlled resuscitator appartusJune 1965Wilson
3114365Apparatus for pulmonary ventilation during anesthesiaDecember 1963Franz
3101708Electronic time cycled respiratorAugust 1963Perry et al.
3033196Artificial respiration apparatusMay 1962Hay
3033195Respirator apparatus and methodMay 1962Gilroy
1169995N/AFebruary 1916Prindle



Primary Examiner:
Gaudet, Richard A.
Assistant Examiner:
Dunne G. F.
Claims:
I claim

1. A lung ventilator adapted to control the volume of respirable gas supplied to a patient irrespective of the duration of the inspiratory phase of the patient's respiratory cycle, of the patient's airway pressure, or of variations in the rate at which gas flows to the patient, including an inhalation passageway connected at one end to a supply of pressurized respirable gas, and at the other end to the patient; an exhalation passageway connected to the patient; a gas flow control valve in said inhalation passageway; a gas flow sensitive transducer in said inhalation passageway and said exhalation passageway adapted to generate signals of which the frequency is proportional to the gas flow rate; means integrating said flow rate signals to produce a signal which is a measure of the volume of gas flowing therethrough; means for closing the said valve when the said integrated signal from said gas flow sensitive transducer in said inhalation passageway reaches a chosen value, and means for reopening the valve and rendering the transducer effective at the beginning of the next inspiratory phase.

2. A lung ventilator as claimed in claim 1, including a two-position, multiple-port valve movable between a `manual` and an `automatic` position, the valve having two of its ports connected to the inspiration and expiration passageways of the ventilator, two ports adapted to be connected to a patient, and the remaining port or ports adapted to be connected to a manual rebreathing device.

3. A lung ventilator as claimed in claim 2, in which the said multiple-port valve is connected to means for displacing it into the manual position when the pressure of oxygen or other selected gas supplied to the ventilator falls below a chosen minimum value.

4. A lung ventilator as claimed in claim 1, in which the signals corresponding to the inspiratory volume flow are fed to an integrator of which the output is fed to a comparator for comparison with like signals corresponding to the desired volume flow, equalisation of the two signals being effective to cause the comparator to generate a changeover signal stopping the inspiratory flow and allowing the expiratory flow to start.

5. A lung ventilator as claimed in claim 4, in which the outlet of the comparator is connected to a device controlling both a valve in the inspiratory flow passageway and an auxiliary valve controlling the position of a valve in the expiratory flow passageway.

6. A lung ventilator as claimed in claim 4, in which operation of the control device is adapted to start a timer when the comparator generates the said changeover signal and which, after a chosen time has elapsed, causes the comparator to be reset and the inspiratory valve to be opened.

7. A lung ventilator as claimed in claim 1, including a minute volume indicator connected to said exhalation integrating means.

8. A lung ventilator as claimed in claim 7, in which connected to the minute volume indicator is an alarm device adapted to operate when the minute volume goes beyond chosen minimum and maximum values.

9. A lung ventilator as claimed in claim 4, including a tidal volume indicator connected to the inspiratory flow integrator.

10. A lung ventilator as claimed in claim 1, in which couplied to the inspiratory flow passageway is a meter for indicating the oxygen content of the gas supplied to the outlet of the ventilator.

Description:
This invention relates to ventilators, and particularly to lung ventilators, which are devices intended to be connected to a patient's airway and designed to augment or replace the patient's ventilation automatically.

The present invention aims at providing a lung ventilator in which the volume of gas supplied to the patient during each inspiratory phase of the respiratory cycle can be chosen and adjusted, irrespective of any variations in the rate of flow of gas to the patient.

By `gas` in this specification is usually meant a mixture of gases, although there might be occasions in practice in which a pure gas, such as oxygen, might be used.

Accordingly the present invention provides a lung ventilator which is as claimed in the appended claims.

The present invention will now be described by way of example with reference to the accompanying drawing, which is a schema of one form of lung ventilator of the present invention.

There are three main types of lung ventilators: volume-cycled, time-cycled and pressure-cycled. Of these the volume-cycled ventilator is the type preferred for long-term ventilation, as is used in intensive care units. However, despite its popularity, the volume-cycled ventilator has disadvantages.

The main advantage claimed for volume cycling is that the ventilator will continue to deliver a chosen volume of gas regardless of changes in compliance of the patient or resistance of the airways. However this is only partly true, in that the actual volume of gas may be less, sometimes considerably so, than the volume which the ventilator indicates as having been supplied to the patient. This discrepancy may be caused by leaks in the various connections and by incorrectly set safety valves or other components.

Conventional volume-cycled ventilators normally use a fixed-volume device, such as bellows or a piston. With these ventilators, the pattern of inspiratory flow is generally fixed, or is adjustable only to a very limited extent. In other words, the limitations imposed by bellows or a piston (with their associated driving mechanisms) restricts the user's ability to alter the flow pattern at will, even though the inspiration/expiration ratio can usually be varied. It is well known that the inspiratory and expiratory flow pattern in mechanical ventilation can affect the efficiency of pulmonary gas exchange, even though the optimum ventilatory flow pattern has yet to be defined. Thus the ability to be able to vary the rate of flow throughout the inspiratory phase of the respiratory cycle, and at the same time to choose the volume to be cycled, would be a considerable advantage, which is offered by apparatus of the present invention.

This includes a mixer 2 to which is connected separate pipe lines for supplying oxygen and air or any other combination of respirable gases. The desired gas mixture passes from the mixer 2 to a device 4 which determines the flow pattern. For example, it may be desirable to maintain a constant flow rate throughout the inspiratory phase. Alternatively it may be desirable for the flow rate to be initially quite high, decreasing after a time to a chosen rate which continues until the end of that inspiratory phase of the respiratory cycle. Other flow patterns may also be required. For convenience, the gas leaving the pattern generator 4 is shown as passing to a separate device 6 for controlling the flow, although in practice the devices 4 and 6 could be combined into a single device determining both the flow rate and the flow pattern. The gas then passes through a valve 8 which is biassed to be open during the inspiratory phase, the valve 8 being controlled by a device 10.

The gas next passes to a sensor 12, which is preferably of the type which develops a signal, preferably electrical of which the frequency is proportional to the gas flow rate, each time a unit volume of gas has passed through the sensor. The signals pass to an integrator or pulse counter 14.

On its way to a valve 16 samples of the gas may be passed into an analyser 18 adapted to display the percentage of oxygen in the gas flowing along the airway 20. This indicator acts as a check on the correct operation of the mixer 2.

The valve 16 is preferably of the two-position, five-port type although other multi-port valves could be used. Two of the ports go to the patient (not shown); one of the ports is in communication with the airway 20; another is in communication with an exhaust line 22, and the fifth in communication with a manual rebreathing device 24. Gas expired by the patient and passing up the line 22 flows through a second sensor 26 which, similarly to sensor 12, passes to a second integrator or pulse counter 27 signals indicative of the volumetric flow through it.

Gas leaving sensor 26 passes through an expiratory valve 28 which is controlled by the pressure of gas in a control line 30, the valve acting as a lightly loaded non-return valve when the pressure in line 30 is below a chosen value, and being forcibly closed to prevent further exhalation when the pressure is above this value.

The pressure in control line 30 is derived from the main airway 20, and an extension 32 of the control line also passes to the valve 16 to bias it to the position in which the valve is in its `automatic` position. The valve 16 is movable manually or automatically from this position to the `manual` position in which the device 24 is able to supply gas to the patient, with airway 20 being blocked. Although this is not shown in the drawing, or described in great detail in the specification, the ventilator may be designed so that upon failure of the oxygen supplied to the mixer 2, the valve 16 is automatically switched over to its `manual` position and an alarm signal generated to alert an operator of the ventilator to the fact that it is operating in the manual mode. However the means by which this can be effected do not form part of the subject-matter of this application and so will not be described herein in greater detail.

Inserted in the control line 30 is a valve 34 also controlled by device 10. The change in pressure in line 30, as a result of actuation of valve 34, is used to operate a pressure-sensitive switch 39 connected to a timer 40.

The integrator 14 supplies a signal, indicative of the volume passing through the sensor 12, to a comparator 36, which receives a similar signal from a preset volume signal generator 38 which the operator can adjust. The comparator 36 supplies an output signal to the control device 10, and is arranged to supply this signal when the measured volume of gas passing through the sensor 12 is equal to the volume preset by device 38.

Operation of control device 10 is arranged to cause switch 39 to supply a signal to an expiratory timer 40 which then supplies a signal resetting the comparator 36 and the valve 8 when a chosen time interval has elapsed since operation of the control device 10.

The integrator 14 is also connected to a voltmeter 46 operating as a tidal volume indicator. During the inspiratory phase of the breathing cycle the integrator 14 increments the reading of voltmeter 46, which reading remains static during the ensuing expiratory phase. At the changeover to the next inspiratory phase the integrator 14 and the meter 46 are reset to zero (by means which is not shown).

The integrator 27 is similarly connected to a second voltmeter 42 acting as a minute volume indicator, which is connected in turn to an alarm device 44. The charge sensed at the appropriate terminal of meter 42 is continually discharged through a leak resistor (not shown). The meter 42 thus settles at a reading determined by the constant leak being balanced (somewhat inexactly) by the pulsiform additions from integrator 27, the meter being damped appropriately. This reading is a measure of the minute volume. Too low a reading, caused as by the patient ceasing to breathe, or the supply of gas falling excessively or ceasing, causes the alarm 44 to be triggered. This happens also when the reading becomes excessive, indicating over-ventilation of the patient.

For convenience, all the components of the ventilator are preferably enclosed in a common housing from which project the ends of the various conduits and airways, and also the control knobs for the adjustable components. The faces of the minute volume indicator and tidal volume indicator are also visible to the operator, so that he has all the necessary indications of the working of the ventilator without being concerned about its internal arrangements.

The ventilator operates as follows:

The mixer 2 supplies to the pattern generator 4 gas having a chosen amount of oxygen. This may range in steps from about 20 percent oxygen to 100 percent oxygen. The pattern generator may provide for continuous adjustment of the flow rate pattern or it may similarly be able to provide any one of a discrete number of patterns. Similarly the flow rate device may provide for any one of, say, six different flow rates to be provided, spanning the range, say, from 10 to 70 litres per minute, although conceivably this could be adjustable continuously over the same range or any other range considered desirable.

During the inspiratory phase the valve 8 is biassed open, as by a solenoid in device 10 operating both valves 8 and 34, as indicated by the broken line 48. When in the `automatic` mode, the gas passing through the valve 8 flows directly through the sensor 12 and the respective passages in the valve 16.

During this phase, the valve 28 is biassed closed by the pressure in control line 30, so that no flow passes from the patient through the sensor 26.

When the signals from the integrator 14 indicate that the volume of gas which has passed through the sensor 12 is equal to the desired volume, then the comparator 36 generates a signal to vary the position of the control device 10. This device 10 is then effective to close the valve 8 and simultaneously open the valve 34, so that the pressure of the gas in line 30 decreases and allows the expiratory valve 28 to open to permit the patient to expire. This pressure rise operates switch 39 and starts the expiratory timer 40 to set the length of the expiratory phase of the respiratory cycle. When this preset time has lapsed, the timer 40 supplies a signal to the comparator to reset it. The control device 10 is also reset, causing the expiratory valve to be closed and the inspiratory valve 8 to be opened, so that the next respiratory cycle is started.

It will be appreciated that the essential components of the ventilator which give it the desired and novel degree of flexibility are the sensor 12; the integrator 14 for measuring the volume of gas supplied to the patient; the comparator 36; the volume control 38, and the control device 10 and its associated valve 8 in the airway to the patient.

As has been mentioned briefly above, in the event of failure of electrical supplies or pressure of the gas supplied to the ventilator, the valve 16 is arranged to be switched automatically to its `manual ` mode. The device 24 may be a rebreathing bag, or self-filling bellows or equivalent device, by means of which the patient may be inflated manually and allowed to expire naturally, as is well-known.

It is usual in lung ventilators to incorporate a safety valve to control the pressure of gas in the system to ensure that the patient is not over-inflated should part of the ventilator malfunction. The safety valve is not shown in the drawing, for clarity, but it would normally be positioned upstream of the sensor 12 so that any gas passing to the atmosphere through the safety valve would not be registered falsely as gas supplied to the patient.

It will thus be seen that the present invention provides a lung ventilator in which the flow of gas to the patient may be adjusted to have a desired pattern during each inspiratory phase, while the tidal volume can be preset to a chosen amount irrespective of any variations in the flow rate or pattern.

The manner in which many components of the illustrated system are actuated has been shown only by way of example. Thus some of the pneumatically operated or biassed components could be actuated mechanically or electromechanically while still being in accordance with the invention.