1. Field of the Invention
This invention relates to systems and methods for the analysis of exhaled breath.
2. General Background
Analysis of a subject's exhaled breath is a promising clinical tool, with potential application in the diagnosis and management of many conditions. For instance, changes in nitric oxide (NO) concentration in exhaled breath can indicate a change in the level of inflammation in the airway of a patient with asthma, indicating an increase in the likelihood of an asthmatic attack. Excessive carbon monoxide (CO) can indicate hemolytic jaundice, and high levels of hydrogen can indicate carbohydrate malabsorption.
It is difficult to build an exhaled breath analyzer because fluctuations in temperature, humidity, breath flow etc. complicate and interfere with the analysis. These difficulties are especially acute when the device is designed to measure trace gases, such as NO, since the sensitivity required for such analyzers also makes the devices much more sensitive to changes in testing conditions. Thus, any device that seeks to quantify trace analytes in exhaled breath must somehow minimize or account for these variables.
In particular, a trace gas breath analyzer must make some provision for changes in the flow rate of breath from the patient. In the past, the clinician or device simply provided feedback to the patient, indicating that the flow rate should be higher or lower. An alternative system alters flow resistance in response to changes in flow rate, thereby attempting to maintain a constant flow rate. See U.S. Pat. No. 6,733,463 (“Moilanen System”).
But these previous systems are far from ideal. The “patient control” method is crude and imprecise, and depends on the patient's ability to adjust flow rate. Such a system would likely be impracticable for wide-scale trace-gas analysis of human breath. It is also difficult to use with children.
Likewise, the Moilanen system is somewhat complex and requires a relatively high number of components, since it depends on a relatively complicated feedback control for operation.
The present invention is a system and method for controlling the flow of a gaseous sample in an exhaled breath analysis system. This invention can be used with systems that quantify a number of analytes, including but not limited to trace gas constituents such as NO.
The present invention has a number of different embodiments, but the common element is the use of a pump or pumps to affect and control the flow rate of the exhaled breath. Two specific embodiments are described, but the scope of the present patent should be determined by its claims, and should not be limited to these two particular embodiments.
The present invention is a system and method for controlling the flow of a sample gas in an exhaled breath analysis system. Two embodiments are described in this patent: a single pump embodiment and a dual pump embodiment. This invention may be used with sensors that have sensing elements that change in response to an analyte in a gaseous sample. Examples of sensing systems and devices that could be used with present invention are provided in U.S. patent applications Ser. Nos. 10/767,709, 10/334,625, and 10/659,408, the disclosures of which are incorporated by reference herein as if set out in full.
The breath analysis begins with the user exhaling into a blow tube 10. Other means of capturing a flow of exhaled breath can be used, such as a mask, etc. See
The breath then travels to a pressure sensor 50 that monitors the pressure within the user's mouth. The pressure sensor 50 should have an operating range appropriate to breath pressure requirements, and in one embodiment this range is 5 to 20 cm H2O. The pressure sensor 50 is used as feedback for the patient, so that the patient maintains pressure in the desired range of 5 to 20 cm H2O. When the pressure reaches a threshold, the first pump 40 switches on. In one embodiment, this threshold is 5 cm H2O, which represents the pressure necessary to close the velum. The upper end of the range, 20 cm H2O, is selected because pressures above that threshold can cause discomfort in some patients.
The breath then travels through an optional first resistance means 60. In conjunction with the second resistance means 70 (described below), the first resistance means 60 may be set to ensure a constant flow rate of 50 cc/sec from the patient. The two resistance means cause the pressure in the patient's mouth to increase, thereby causing the velum to close. The first resistance means 60 may be a fixed orifice, and in one embodiment this fixed orifice has a round aperture of approximately 0.11 cm diameter. Other conventional resistance means could be used instead of or in addition to the fixed orifice. For purposes of this patent, “resistance means” or “resistor” shall refer to a structure that creates resistance. This first resistance means 60 is not necessary, but may help to “tune” the system to the pump specifications.
After the first resistance means 60, the circuit splits into two streams: a primary stream 20 and a side stream 22. See
The primary stream 20 contains a second resistance means 70 that produces a resistance Rp. In one embodiment, this resistance means 70 may be able to produce a variable resistance, as described below. The second resistance means 70 may be a motor-controlled needle valve, a solenoid controlled needle valve (as used in mass flow controllers), a manual needle valve, a fixed resistance orifice, or any other means of producing the desired resistance.
The side stream 22 contains a side stream valve 24 that controls whether this stream is open or closed. The side stream valve 24 may be a solenoid valve or other appropriate open/close valve.
After a predetermined amount of time, the side stream valve 24 opens, and while the side stream is open, the breath flow moves in parallel through the two streams. In one embodiment, the side stream 22 is open for the period of time between 7-10 seconds after exhalation into the blow tube begins. Thus, in this embodiment, for the first seven seconds, all the exhaled breath passes through the primary stream 22, then through the pump 40, and then is vented into the ambient atmosphere.
The side stream 22 contains a sensor 30. The sensor 30 creates its own resistance, Rs. Other components, including a carbon dioxide scrubber, may also be placed in the side stream 22. The inlet and outlet of the sensor 30 may have check valves 32, 34 to prevent leakage. See
There are two different techniques to maintain a constant flow rate from the patient when the side stream 22 is opened. In the first version, the primary stream 20 has a second resistance means 70 that varies its resistance to ensure a total flow rate of 50 cc/sec (or other desired rate) from the patient throughout the entire exhalation. The resistance from the second resistance means 70 will be referred to as “Rp,” where the p stands for pump. The resistance from the sensor (Rs) and the other components of the side stream 22 has a constant value, but in this embodiment, Rp has a variable value. When the side stream 22 is closed, the value of the second resistance means is Rp1, but when the side stream is open, the value of the second resistance means changes to Rp2. The values Rp1 and Rp2 are chosen so that the sum of the flow rates through the primary stream 20 and the side stream 22 is equal to the flow rate through the primary stream 20 when the side stream 22 is closed. In setting the values Rp1 and Rp2, the resistance from the other components in the circuit (such as Rs and the first resistance means 60) must be taken into account, and the pump voltage must also be considered.
For instance, in one embodiment, the value of Rp may change as described below:
In this example, ΔP stands for the change in pressure across the pump, R1 is the resistance from the first resistance means, Rp1 and Rp2 are the resistances from the second resistance means 70 when the side stream valve 24 is closed and open, respectively, Rs is the resistance from the sensor 30, and i is the total flow through the system and from the patient's mouth.
As indicated above, in one embodiment, Rp1 and Rp2 are chosen so that a constant flow rate of 50 ml/s is maintained throughout exhalation. In this embodiment, the desired flow rate through the sensor 30 is 8 ml/s, so Rp2=(8/42)*Rs. Since total flow through both streams should equal the flow through the primary stream when side stream 22 is closed, Rp1=(42/50)*Rp2. When Rp is variable, as in this embodiment, the second resistance means 70 may be a solenoid needle valve (as used in mass flow controllers), or a motor-controlled needle valve, or a pinch tube valve, or any other suitable resistor that can change its resistance.
Thus, in this embodiment, when the side stream 22 is opened during the final 3 seconds of exhalation, 8 ml/s passes through the side stream 22, with the remainder (42 ml/s) of the breath passing through the primary stream 20. This yields a value of 0.29 for Rp2, according to the equation Rp=Fs*(Fs/Fp), where Fs is the flow rate through the sensor in mL/min, and Fp is the pump flow rate in mL/min.
In the second technique, both Rp and Rs are fixed (Rp=8/42 Rs), and then during the period of time when the side stream 22 is open, the pump varies the pressure drop to accommodate the change in overall circuit resistance resulting from the opening of the side stream 22.
For instance, the following table illustrates certain values in the system when the voltage of the pump is varied:
In this example, ΔP stands for the change in pressure across the pump, R1 is the resistance from the first resistance means, Rp1 is the resistance from the second resistance means 70, Rs is the resistance from the sensor 30, and i is the total flow through the system and from the patient's mouth.
As shown in
The first pump 40 is downstream from the joinder of side stream 22 and the primary stream 20, so that it can control the overall flow of the system, and not each stream individually. See
By placing the first pump 40 downstream from the sensor, the present system avoids the possibility that output from the pump 40 would contaminate the sensor 30. When two pumps are used (as described below), both pumps would typically be placed downstream from the sensor 30. However, it is also possible for the pump or pumps to be placed upstream from the sensor 30.
In this embodiment, the system has two pumps: a first pump 40 (as described above), and a second pump 80. See
Both flow rate control methods described above (variable resistance and variable pump operation) may be used in conjunction with the dual pump embodiment.
In the dual pump embodiment, it may not be necessary to employ a side stream valve 24. Instead, the second pump 80 may be used to control flow to control flow into the side stream 22.
Also, in the dual pump embodiment, side stream 22 and the primary stream 20 may not rejoin, but instead may vent through separate exhaust points. See
Side Stream/Stopped Flow Analysis
As noted above, the present system uses a side stream 22 to direct breath flow through the sensor 30. Use of a side stream 22 allows analysis of a relatively small breath sample, which in turn allows the creation of a smaller, more conveniently-sized sensing device. For instance, use of a side stream 22 allows the division of a 50 ml/s exhaled breath stream into a 8.0 ml/s side stream 22 and a 42.0 ml/s primary stream 20. The smaller side stream 22 can be used to supply exhaled breath to a smaller sensor 30 than would be necessary if the entire breath stream were analyzed.
Also, as noted above, the side stream 22 is opened only after a period of time, such as 7 seconds after exhalation begins, to allow concentration of the exhaled analyte to stabilize. Breath will then flow into the side stream 22 and sensor 30 for a fixed period of time, such as 3 seconds.
After the expiration of this period of time, the side stream 22 can be closed to allow the sensor enough time to interact with the exhaled breath. In other words, the sensor 30 will “incubate” a sample of stopped exhaled breath for a period of time. In one embodiment, this “incubation” period or analysis period would be approximately 1 minute. After the incubation period, the sensor 30 would then be analyzed to determine concentration of the analyte. By allowing the sensor 30 to interact with the stopped exhaled breath for a relatively extended period of time, the present invention allows the use of sensors that have response times that are too slow to analyze a moving stream of breath.
Also, by opening the side stream 22 for a few seconds, the present invention allows the sensor 30 to receive multiple cycles of exhaled breath before the flow is stopped. For instance, if the sensor 30 has a volume of 5.0 ml, and if the side stream 22 provides 8.0 ml/s of exhaled breath to the sensor for 3 seconds, then approximately 24.0 ml of breath will have passed through the sensor before the final 5.0 ml is trapped. This represents three complete cycles through the sensor before analysis begins, thereby completely flushing the sensor of whatever gas was inside the sensor before capturing the breath.
The “stopped flow” aspect of the present invention provides a number of advantages. By stopping the flow of breath through the sensor during analysis, the present invention creates a stable analytical environment, with no changes in pressure or flow during the entire analysis period. Changes in pressure or flow could create artifacts that interfere with analysis.
A stopped flow system can also accommodate slow sensors that detect trace gases. By stopping the flow, the system creates a stable testing environment that can be maintained for a much longer period than is possible for a flowing system. In one embodiment, the analysis period is approximately one minute, although much longer periods are also possible.
The present system can be used for analysis of many different analytes in exhaled breath, including trace gases like NO. For purposes of this patent, “trace gas” includes gases with concentrations below 1 part per million. In one embodiment, the system can be used in a conjunction with a sensor consisting of cytochrome-c in a sol-gel to measure NO.
One skilled in the art will appreciate that the present invention can be practiced by other than the preferred embodiments, which are presented for purposes of illustration and not of limitation.