CA2064892A1 - Shutterless optically stabilized capnograph - Google Patents

Shutterless optically stabilized capnograph

Info

Publication number
CA2064892A1
CA2064892A1 CA002064892A CA2064892A CA2064892A1 CA 2064892 A1 CA2064892 A1 CA 2064892A1 CA 002064892 A CA002064892 A CA 002064892A CA 2064892 A CA2064892 A CA 2064892A CA 2064892 A1 CA2064892 A1 CA 2064892A1
Authority
CA
Canada
Prior art keywords
infrared
detectors
detector
signal
filter
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002064892A
Other languages
French (fr)
Inventor
Daniel S. Goldberger
James R. Braig
Mark Yelderman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ethicon Inc
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US07/522,177 external-priority patent/US5081998A/en
Priority claimed from US07/522,208 external-priority patent/US5095913A/en
Application filed by Individual filed Critical Individual
Publication of CA2064892A1 publication Critical patent/CA2064892A1/en
Abandoned legal-status Critical Current

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/31Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
    • G01N21/35Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
    • G01N21/3504Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light for analysing gases, e.g. multi-gas analysis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/08Detecting, measuring or recording devices for evaluating the respiratory organs
    • A61B5/083Measuring rate of metabolism by using breath test, e.g. measuring rate of oxygen consumption
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01JMEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY
    • G01J1/00Photometry, e.g. photographic exposure meter
    • G01J1/10Photometry, e.g. photographic exposure meter by comparison with reference light or electric value provisionally void
    • G01J1/20Photometry, e.g. photographic exposure meter by comparison with reference light or electric value provisionally void intensity of the measured or reference value being varied to equalise their effects at the detectors, e.g. by varying incidence angle
    • G01J1/22Photometry, e.g. photographic exposure meter by comparison with reference light or electric value provisionally void intensity of the measured or reference value being varied to equalise their effects at the detectors, e.g. by varying incidence angle using a variable element in the light-path, e.g. filter, polarising means
    • G01J1/24Photometry, e.g. photographic exposure meter by comparison with reference light or electric value provisionally void intensity of the measured or reference value being varied to equalise their effects at the detectors, e.g. by varying incidence angle using a variable element in the light-path, e.g. filter, polarising means using electric radiation detectors
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01JMEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY
    • G01J5/00Radiation pyrometry, e.g. infrared or optical thermometry
    • G01J5/10Radiation pyrometry, e.g. infrared or optical thermometry using electric radiation detectors
    • G01J5/12Radiation pyrometry, e.g. infrared or optical thermometry using electric radiation detectors using thermoelectric elements, e.g. thermocouples
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/31Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
    • G01N21/314Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry with comparison of measurements at specific and non-specific wavelengths
    • G01N2021/3166Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry with comparison of measurements at specific and non-specific wavelengths using separate detectors and filters
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/12Circuits of general importance; Signal processing
    • G01N2201/126Microprocessor processing

Abstract

Methods and apparatus for constructing optically stabilized, shutterless infrared capnographs are disclosed. The capnographs of the present invention provide the absolute concentration of the constituents of the respiratory airstream of a patient, without the thermal drift problems normally associated with thermopile detectors, thereby providing a device with a high degree of accuracy.
The present invention eliminates the need for a mechanical shutter to modulate the incident infrared beam and the need for a modulated source, thereby increasing the reliability and response time of the devices disclosed. Capnographs which are substantially unaffected by changes in the ambient temperature at which they operate are provided by connecting pairs of filtered (60, 61, 62, 16, 18, 26, 28, 36, 38) thermopiles (12, 14, 22, 24, 32, 34) in series and processing the resulting differential signal (242).

Description

1 PAT~NT

8~TTER~ESS OPTICALLY 8$ABILIZED CAPNOG~APH

.

~ACRGRO~ND OF ~ INVEN$ION

Field of the Invention The present invention relates to methods and apparatus for . .
continuously determining the concentration of the constituents of the respiratory qases of a patient. Most preferably, the apparatus of the present invention is employed to monitor the end ~ ~-tidal CO2 and N2O concentrations of a patient.

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Description of the Prior Art It is frequently of critical importance to monitor the concentration of carbon dioxide (CO2) in the gases inspired and expired from a patient under anesthesia, for expired CO
concentration is a reliable indicator of the carbon dioxide concentration in the arterial blood. In a clinical setting, monitoring expired CO2 prevents malfunctions in anesthesia r breathing apparatus from going undetected and delivering xcessive a~ounts of C2 to the patient. Rebreathing of anesthetic gases is very cost effective and environmentally desirablo, but accurate C02 concentrations are difficult to maintain in the patient circuit without a concentration monitor.

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~, - ' ; .... . '. ' .` ~ , WO9l/0320~ PCT/~S90/04875 It is ~4 th:t by directlng infrared radiation through a sample of a gaseous mixture and measuring the incident radiation illuminating a detecting device, a measure of the infrared absorption of the gas can be obtained. Electrical signals produced by a detecting device in such a manner are thus indicative of the infrared absorption of the gas and can be processed to produce an output indicating the concentration of one or more of the constituents of the gas being analyzed. This type of gas analyzer operates on the principle that various gases exhibit substantially increased absorption characteristics at specific wavelengths in the infrared spectrum and that higher gas concentrations exhibit proportionally greater absorption.
Prior art infrared gas analyzers such as that described in U.S. Patent No. 4,648,396 to Raemer utilize thermopile detectors to analyze gas concentrations. A thermopile detector is comprlsed of a number of thermocouples. Thermal detectors such as thermopiles are used primarily for infrared sensing and respond to the total incident energy illuminating them. The number of thermocouples must be sufficient to develop enough voltage to develop a suitable signal to noise ratio. A
thermistor is used to calculate the Seebeck coefficient, which relates the voltage developed by the thermopile to the temperature differential between the "hot" and "cold" junctions of the thermopile. This coefficient is used to scale the output signal of the detector to indicate absolute gas concentration values.
Similarly, in U.S. Patent No. 4,772,790, Aldridge discloses a non-dispersive optical gas analyzer which uses thermopiles as . , 3 ',~ ~ -~ - , . . : :

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.,. ~. ': ' w091/03204 PCT/~'S90/04875 3 2Q~ '~,92 optical detectors. The thermopiles are formed of an array of interconnected thin films of dissimilar metals deposited on a heat conductive substrate to form a plurality of thermocouples.
The array is configured in such a manner that a number of the thermocouples are employed to compensate each thermopile output signal for changes in ambient temperature. U.S. Patent 3,539,804 Billetdeaux et al. also relates to an infrared absorption apparatus, but unlike Aldridge, Billetdeaux et al use a rotatable neutral attenuator as a zeroing mechanism in assembly balancing of a CO2 detector.
Thermopile detectors as a class are known to suffer from thermal drift. Thermal drift causes a slow variation in the D.C.
voltage output of the detectors and leads to measurement inaccuracies. Raemer overcomes this problem by using A.C.
lS coupling between the thermopiles. This solution to the thermal drift problem, however, renders the resulting analyzer incapable of measuring absolute, steady state, gas concentrations.
Instead, such devices are merely able to respond to chan~es in the concentrations of the gases being measured.
One method which attempts to obtain absolute gas concentrations involves modulating, or "chopping", the incident energy beam. This technique is taught in U. S. Patent No.
4,423,739 to Passaro. In order to accomplish the required modulation, mechanical means such as a chopper are frequently 2S employed. The resulting analyzer is large, and is thus subject to failure as the moving parts of the beam modulation apparatus we~r. Such failure may have catastrophic consequences rendering the analyzer inoperable.

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,:, - . , .- ,. : -w091/03~04 ~9~ PCT/1'59~/04875 An alternative method of modulating an energy beam is to construct a modulated source. Devices of this type are disclosed ~;y~;
in U.S. Patent No. 3,745,349 to Liston, for example. However, to date, analyzers employing modulated sources have suffered from slow response times due to the relatively long period required for the infrared emissions to decay after the excitation power is removed. Another shortcoming of modulated sources, familiar to those skilled in the art, is the relative instability of their energy output.
10In addition, the imbalance between the excitation signals of two detectors has been utilized as a detection mechanism in the field of infrared motion detectors. In these devices, two detectors are arranged and their signals combined so that a null s signal results when the detectors are identically excited. Any change in the environment that causes the output signal of one detector to change by an amount different than that of the other detector results in a non-zero differential signal. Thus, by subtracting the two output signals from two identical detectors an imbalance in the input excitation of the two detectors can be measured. An application of the method of subtracting two detector output signals, perhaps in an attempt to stabilize thermal drift, involves totally blocking one of the thermopile det-ctor~ with metal foil. This approach, however, is undesir~ble because of results in uneven heating of the substrate, thus causing an error signal to be introduced into the output.
Thus, at the present time, the devices available provide absolute concentrations with the trade-off of either decreased - .
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-206~8Y2 5reliability in the case of mechanically shuttered devices, or slow response times in the case of modulated source devices.
Eliminating either of these drawbac~s using conventional thermopile detectors results in a device prone to inaccuracies due to thermal drift, or one incapable of determining absolute concentrations if the thermal drift is stabilized using A.C.
techniques. Therefore, a reliable gas analyzer using thermopiles that is both immune to thermal drift and capable of providing absolute gas concentrations would be highly desirable.

~UMMARY OF TH~ INVENTION
It is an object of the present invention to provide methods and apparatus for detectinq the absolute concentration of the constituents of a gas stream using thermopile detectors. Another object of the present invention is to eliminate the thermal drift from which thermopile detectors are known to suffer, while retaining the capability of measuring absolute gas concentrations and the like.
It is a further object of the present invention to accomplish the abcve objects without modulating or "chopping"
the incident e..ergy beam.
Accordingly, the present invention provides a shutterless capnograph comprising an apparatus which has no moving parts, which doea not require a modulated source of infrared radiation, and which does not suffer from thermal drift, thereby providing a device which overcomes the limitations of the prior art. The improv ments provided by this invention are arrived at through a nov-l optical stabilization technique applied to thermopile ~- . .
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wo 91~03204 PCl'tl,lS90/04875 ?,Q~4~9 ` 6 detectors. A preferred em~odiment of the invention provides a highly accurate, stable, reliable, light-weight and economical infrared capnograph which will permit increased clinical and diagnostic monitoring of the absolute concentrations of carbon dioxide, nitrous oxide or other gases present in the expired airstream of a patient.
The present invention provides apparatus comprising one or more channels of a shutterless infrared gas analyzer for detecting the concentration(s) of at least one gaseous component of a substantially gaseous flow stream. The apparatus comprises at least two infrared detectors which produce electrical signals when illuminated by optical energy and means for illuminating the detectors with infrared radiation. Means for directing at least a portion of the gas being analyzed between the detectors and the infrared source is provided along with means for attenuating the infrared energy iiluminating at least one of the detectors and circuitry for combining the signals produced by the detectors to produce an optically stabilized signal. If desired, the apparatus may further comprise additional detectors, attenuators, and circuitry, sufficient to comprise separate channels of a multi-channel device. The apparatus may also function in conjunction with a host processor for storing, processing, and displ~ying the measured information.
In accordance with the invention, an infrared energy detector is provided which incorporates a novel optical stabilization technigue applied to thermopile detectors. The r-~ulting detector readily measures the intensity of recsived infrared energy from a source of infrared energy. From the .~ `.

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7 PA~NT
detected energy levels, information as respiratry airstream constituent concentrations or body temperature may be determined.
In a preferred embodiment, the energy detector has first and second infrared detectors positioned to receive infrared energy from the infrared energy source and to generate corresponding electrical signals. Improved performance is realized by providing means for distinguishing the desired infrared energy signal components from undesired thermal effects included in the energy measurement.
As mentioned above, the drift usually associated with thermopile detectors is produced by a variation in the reference junction temperature. In normal construction, a thermopile detector is comprised of a series of thermocouple junction pairs.
One element of each pair is attached to a substrate (typically lS ceramic) and called the reference junction while the other element is unattached, suspended over an opening, and is called the sensing element. Incident radiation illuminates the suspended sensing element and raises its temperature. A voltage develops that is related to the difference in temperature between the suspended and substrate attached elements. Drift arises, however, because the incident radiation and room temperature variations change the temperature of the reference junctions.
Th- temperature differential between the sensing (hot) and reference (cold) junctions is thus altered; this condition in turn causes the output voltage to change, or drift.
A preferred embodiment of the present invention incorporates a substantially identical pair of thermopile detectors mounted on the same ceramic substrate and connected in series opposition.

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. -'' : - ' ' ' ' WO91/03204 PCT/~S90/04875 In th ~ ~ ~91guration, balanced and equal incident radiation illuminating the pair will produce no signal. Because the reference junctions of both detectors are on the same ceramic substrate and at substantially the same temperature, a drift in substrate temperature will produce no discernible change in output signal, thereby overcoming the above-mentioned problems.
In order to make the system respond to incident radiation, an optical filter, or attenuator, with a transmission coefficient of approximately 0.50 (i.e., 50% transmission) is placed over one of the thermopile elements in the pair. With the filter in place the system responds to incident radiation but is substantially insensitive to other thermal changes. Also, in the present invention the output signals of the two thermopile detectors are subtracted. This is done not for the purpose of measuring any imbalance in the signals exciting the detectors, but rather to eliminate the effect of a variation in the background signals.
For example, variations due to thermal drift are cancelled since they are common to both detectors.
The problem of uneven heating described above in connection with the method of blocking one of the detectors is eliminated in the present invention by utilizing attenuation filters that do not cause uneven heating of the substrate. These filters have known but different transmission coefficients so that the incid-nt excitation signal can be accurately determined from the differential signal, as set forth in greater detail below.
In order to permit the analysis of specific gases, optical bandpass filters which permit the transmission of wavelengths within a specified bandwidth (i.e., that absorbed by the gas of E~;` - -. ~ .. .. . . . .
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'~ '- ' ', : ' Wo9l/03204 PCT/US90/04875 interest) are disposed betwe n the detecto9 2 and the gas directing means, thereby filtering the radiation prior to its striking the detectors. Since the center wavelength and bandwidth of optical filters vary with temperature, thermal drift should be considered when designing the optical bandpass filters.
A preferred method for selecting the bandpass filters is described herein.
Circuitry for processing the signals produced by the detectors converts these signals into a ratio which is related to the zbsolute concentration of the gas constituent being measured. As a result, the capnograph of the present invention is substantially unaffected by changes in the ambient temperature of the environment in which it operates through the action of the neutral density filters. The technique described above for combining and processing the detector signals is referred to as "optical stabilization" herein.
A capnograph made in accordance with the present invention may further comprise additional pairs of thermopile detectors, attenuators, and optical bandpass filters, and such additional circuit means so as to form a multichannel device for determining the concentrations of more than one gas constituent. In such a multichannel embodiment, each of the channels has an optical f~lter permitting the transmission of radiation within the absorption bandwidth of the constituent being monitored.
A capnoqraph system made in accordance with the present invention may also have a host system for collecting and processing data collected by the detectors. Such a capnograph system may also include a device for indicating the absolute ~ -' ' - ' ' ~ .

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wo 91/0~ g~9~ PCT/US90/048'5 ~ , ~, , 10 concentration of the constituent or constituents being monitored, thus providing the necessary concentration information in a usable form. -A preferred infrared energy detector for use in a capnograph made in accordance with the present invention is also disclosed.
The detector uses paired thermopiles preceded by an analytical or reference bandpass filter, with a neutral density filter also placed in the optical path of one detector in the pair. Thus, two channels -- one analytical and one reference -- are preferably provided to permit measurements to be taken while the background effects are cancelled.
Most preferably a capnograph made in accordance with the present invention will be used to determine the absolute concentrations of carbon dioxide and/or nitrous oxide in the inspired and expired airstream of a patient. However, the optically stabilized detectors disclosed need not be so limited, and may be utilized to determine the concentrations of any of a number of constituents, as will be apparent to one skilled in the art from the following description.

B~ DF8CRIPTION OF TBF D~A~ING8 FIG. 1 is a foreshortened isometric view of the thermopile detector assombly of the present invention;
FIG. 2 i8 a partially schematic plan view of a gas analyzer :
and related circuitry, constructed in accordance with the present invention;

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FIG. 3 is a schematic of further circuitry, illustrating the use of the present invention in conjunction with a host computer;
FIG. 4 is a schematic illustration of a detector and its optical path, constructed in accordance with the principles of the present invention;
FIG. 5 is a schematic representation of the processing performed on the signal detected by the apparatus of FIG. 4:
FIG. 6 is a perspective view of a detector constructed in accordance with the schematic illustration of FIG. 4; and FIG. 7 is an exploded view of the detector of FIG. 6.
FIG. 8 is a schematic representation of an alternate embodiment of the detector of the present invention.

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A. Optically Stabilized Thermopile Detector FIG. 1 depicts a typical thermopile detector construction.
It can be seen that such a thermopile detector is a group of thermocouples connected in series. The present invention utilizes a first set of thermocouples, comprising a first thermopile 12, and a second set of thermocouples, comprising a second thermopile 14, both preferably mounted on a common ceramic substrate 10, as shown. The hot, or sensor, junctions of the thermocouples are typically denoted ~, while the cold, or reference, junctions are denoted C. Most preferably, the thermocouples 12 and 14 are the type comprising a metallic circuit deposited upon a polyester film, such as Mylar, or other suitable substrate. A preferred embodiment utilizes thermocouples having a substrate thickness of 1 mil.
Also shown in FIG. 1 is the placement of neutral density (attenuation) filters 16 and 18, each of which has a different transmission coefficient. ~ypically, filter t6 has a transmission coefficient of 1.00 and filter 18 a transmission coefficient of 0.50.
In a preferred embodiment, detector 12 is electrically connected to detector 14 in series opposition. The resulting differ nce signal will only be indicative of the incident radiation. Signals caused by substrate temperature changes will cancel, provided the temperature is uniform across the substrate.
Thi8 i8 discussed more fully in the ~athematical derivation provided below.

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Thus, in a preferred embodiment, the thermopile detectors 12 and 14 are "optically stabilized~. This design overcomes the requirement for source modulation described above by rendering the detector substantially immune to thermal drift. Since each of the thermopile detectors 12 and 14 is exposed to the same incident energy beam but has different attenuation filters 16 and 18 in line with that energy, the differential signal from the two detectors is therefore related only to the incident energy and the transmission coefficients of the neutral density attenuation filters. The stabilization technique disclosed by the present invention is useful with a variety of detectors, such as the Model DR34 manufactured by Dexter Research Inc., Ann Arbor, Michigan. Moreover, since the optically stabilized detectors of the present invention are sensitive to a wide range of lS wavelengths, and are relatively inexpensive and rugged, they can be beneficially used in a shutterless infrared capnograph for monitoring respiratory gas.
In FIG. 4, the optical path of an embodiment of a detector 200 constructed in accordance with the principles of the present invention is shown. Infrared energy is emitted from an IR source 300 and passes through the gas being analyzed, which in this example is C02. Some of the infrared energy is absorbed by the gas ~n front of the IR source 300, and the remainder of the infrared energy impinges upon a group of filters, including a neutral density filter 210, an analytical C02 filter 212, and a reforence filter 214. The neutral density filter 210 uniformly attenuates all wavelengths of energy which are incident upon the filter. The analytical C02 filter 212 is a bandpass filter which ;

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passes a narrow band of energy, including those wavelengths absorbed by CO2. The reference filter 214 i5 also a bandpass filter which passes a band of energy excluding those wavelengths absorbed by CO2.
It is seen that the neutral density filter 210 overlaps or shadows the subsequent analytical and reference filters 212 and 214, as well as two of the thermopile detectors 216 and 218, C02 detector B 220 and reference detector B 222. Thus, each detector A 216 and 218 will receive energy which has been transmitted by its respective analytical filter 212 or reference filter 214, but not the neutral density filter 210. Each detector B 220 and 222, on the other hand, receives energy passed by its respective analytical filter 212 or reference filter 214 as well as the neutral density filter 210. Following the filters is an aperture or window 230 which transmits energy to only the detector areas of the substrate on which the detectors are formed. The outputs of the detectors are passed to a processor 240 for the production of an output signal 242 representative of the concentration of C2 in the gas being analyzed.
A main purpose of the neutral density filter 210 is to provide signals which allow the desired siqnal to be distinguished from signal interference such as background (local thermal) effects. A number of attempts have been made in the prior art to deal with these effects. For instance, U.S. Patent No. 4,772,790 to Aldridge attempts to isolate these effects by using ten thermopiles for each detector channel, with only a central portion of the area of the thermopiles being used to develop a usable signal. Tn addition, ~.S. Pat. 3,539,804 to ~;. . . . .. .
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15 206~892 Billetdeaux et al. attempts to deal with the problem through heating and shielding of the detector, and also includes a rotatable neutral attenuator as a zeroing mechanism in assembly balancing of a co2 detector. By contrast, in an embodiment of 5the present invention, local thermal effects are eliminated by developing signals resulting in their cancellation when the signals are combined.
For instance, an examination of the CO2 channel reveals that the CO2 detectors A 216 and B 220 are in close proximity to each 10other and hence experience similar effects from background and other local radiation sources. Each detector produces an output signal containing a component I, the desired incident infrared ;
signal, and a component b due to background effects. Absent the - `:
presence of the neutral density filter 210, the CO2 detectors 216 15and 220 would produce signals of the form:
Det. A = R(I. + b), and Det. B = R(Ib + b), -where R is the response of the detectors.
It is desired to maximize the desired signal component I, 20which may be done by selecting a neutral density filter 210 which i8 about 100% transmissive at the absorption wavelength for C2-In this case A would equal B. The signal component I would be maximized but the difference of the two detector output signals ~ ~ `
would yield zero. Correspondingly, if the neutral density filter `~
25were chosen to be a 100% blocking filter (i.e., 0% trans~issive, ;
Ib~0) at the absorption wavelength, their difference would be A -B - RI,. This would have the undesirable effect of shadowing detector B 220 from all radiation from the IR source 300, thereby :. . , ' ' ~
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blocking detector B 220 from reception of incident energy, and would further set up an undesired thermal differential between the two detectors. Moreover, neither of these two choices leads to the ability to distinguish and eliminate background effects.
If, however, the neutral density filter 230 is chosen to have a transmissivity of about 50%, for instance, the desired incident energy component I would be differentiated and the background effects would substantially cancel. A neutral density filter of this character would produce signals of the form:
Det. A = R(I ~ b), and Det. B = R(0.5I + b).
Thus, when the difference of A minus B is taken, the result is 0.SIR with the background effects b cancellinq. Other transmissivity characteristics may be chosen in consideration of incident energy levels and the thermal effects of shadowing by the neutral density filter 210. For example, a 0% transmissive filter may be used.
The details of the processor 240 of FIG. 4 are shown in FIG
5. The output signals of the A and B detectors 216 and 220 for the CO2 and for the reference channels 218 and 222 are respectively subtracted at subtractors 242 to eliminate background radiation and substrate temperature effects, as explained immediately above. In a preferred embodiment of the pr-sent invention, this subtraction step 242 is accomplished by connecting the thermopile detectors in series opposition, so that the subtraction of their outputs i8 inherent in their interconnection as shown in FIG. S. A ratio 244 is then taken of the incident signals after this cancellation of thermal .. . .

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effects. The ratio 244 of the analytical and reference signals eliminates proportionate effects of spurious absorption, such as those resulting from the accumulation of undesired particulate matter on the components of the detectors. For example, for an incident radiation signal having a normalized value of 0.8 CO2 and filters which are contaminated with substances which absorb some of the radiation being measured, the transmissivity of the optical paths is reduced to 0.9 of full transmissivity. The output signal would thus be the product of these losses, or 0.72 -CO2. When the reference channel is subject to the same contamination, which may be substantially achieved by close proximity of the detectors and filters, the same factor of 0.9 would be present in signals of the reference channel. Hence, the ratio of the CO2 and reference signals would contain the 0.9 factor in both the numerator and the denominator for a ratio of one, eliminating the effects of contamination.
Computations are made on the calculated ratio to further refine the measurement of CO2. The measurement of absolute substrate temperature, provided by the thermistor 246 in the detector, and the appropriate Seebeck coefficient 248 are factors taken into consideration in this computation. The temperature measurement is incorporated into the present invention as shown in the functional block diagram of FIG. 5. As will be understood by those of ordinary skill, the resultant measurement of CO2 is obtained by solving the well-known Bier's Law equation which is of the form I ~ IOe~~', where Io is a constant coefficient, x is path length, ~ is the absorption coefficient for CO2, and c is concentration. The reference channel yields a value for I, since ~ , : : , :
.. . . . . . .
- . . .. , .~ . . .. -.:,. .

:, ,~ - : , ' - . '.

- ,, the absorption coef f icient and concentration of CO2 in the reference channel are zero by reason of the elimination of CO2 wavelengths from the reference filter passband. The detector output signal supplies the value for I, and the equation is solved for c, the concentration of CO2 in the gas being measured.
The above computations are preferably performed by a host processing system of the type described below with respect to FIG. 3.
In a preferred embodiment, a second analytical channel is employed for N2O. This channel is identical to the CO2 channel in FIG. 4, except that the analytical filter 212 is chosen to pass wavelengths representative of the absorption of infrared energy by N2O instead of CO2. The outputs of the A and B
detectors for the N2O channel are combined to eliminate background and substrate thermal effects and the reference channel outputs are combined to yield a measurement of N2O
concentration, as in the COz computation set forth immediately above. In addition, such N2O concentrations may be used in accordance with the techniques taught by Severinghaus, M.D., Larson, M.D. and Eger, M.D. in an article entitled "Correction Factors for Infrared Carbon Dioxide Pressure Broadening by Nitrogen, Nitrous Oxide and Cyclopropane" in Anesthesiology, May-June, 1961, pp. 429-432, to correct for collision broadening rrors induced in the CO2 gas concentration computation by nitrous oxide.
FIGS. 6 and 7 respectively illustrate in perspective assembled and exploded views a detector constructed in accordance with the present invention. The detector 200 employs the same ~ .
-~ - .

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'~' - ' , ' ' ' . , WO9l/03204 PCT/US90/04875 2~ 892 principles and optical paths shown in FIG. 4. As shown in the perspective of the assembled detector 200 shown in FIG. 7, the neutral density filter 210 is disposed above the reference filter 214 and the analytical filters 212 and 213. In the embodiment of the present invention shown, analytical filters 212 and 213 selected to analyze C02 and N20 are provided, as well as the reference filter 214. Each of these three filters is "shadowed"
or blocXed by the neutral density filter 210 as explained above with reference to FIG. 4.
Further details of the construction of the detector are shown in the exploded view of the infrared detector 200 in FIG.
7. Beneath the filters 210, 212, 213, 214 is the filter aperture -230. The thin film thermopile detectors 216, 218, 220 and 222 are sandwiched between two ceramic spacers 215 and 225.
In FIG. 7, the N20 detectors 224 and 226 are not visible.
A foil background 245 is provided beneath the ceramic spacer/thermopile sandwich to block the further passage of the incident radiation, but it allows heat to be conducted through ;
the device. Finally, beneath the foil bac~ground 245, a thermistor 246 is disposed which, as explained above, provides an absolute temperature indication. The above-mentioned components are mounted on a T0-8 12-pin header 250, as shown.
Wh1le the illustrated embodiments are shown to employ th2rmopile detectors, the principles of the present invention may also be applied through the use of other infrared detecting d-v~cQs, such as thermistors, thermocouples, pyroelectric detectors, 6O1ay cells, and PbSe photodetectors, for instance.

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However, the arrangement shown has the benefit that it i8 easy to manufacture, is small in size and light in weight.
:, :
B. Mathematical Derivation The signal or voltage output, S, of a thermopile detector can be expressed as: -S = (T * I * R) + B, ~;~
where T is the filter transmission coefficient, assuming the filter is between the detector and the energy source, I
represents the incident energy of the source, R is the responsivity of the detector, and B is the component of the signal attributed to background "noise", including room temperature and detector package temperature variations. In a preferred embodiment of the present invention, two detectors 12 and 14 are mounted on a common substrate 10 as shown in FIG. 1, ~
creating a condition wherein the value of B for each detector is -~ ;
equal. The detectors 12 and 14 are used to simultaneously -monitor an incident energy beam. Filters 16 and 18 having known but different transmission coefficients are placed between each detector 12 and 14 and the source of incident energy.
The two equations describing the outputs S1 and S2 of the two detectors 12 and 14 are combined and solved for I, yielding the ~ollowing eguation, which i8 independent of the value of B:
Sl -- S2 2S I =
(T~ * R~) - (T2 * R2) In a most preferred embodiment, the numerator of the above equation, S~ - S2, which represents the difference signal, i8 computed by connecting the detectors 12 and 14 in series ... .
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WO91/03204 PCT/~S90/04875 21 2 ~ ~ ~ 8 9 2 opposition. It should be apparent to one skilled in the art, however, that the difference signal could be calculated using a digital computer or other electronic circuit. Tpe equation demonstrates that the stabilization technique of the present invention eliminates the background effects term, B, from-the final output of the circuit, thereby rendering a device substantially insensitive to room temperature effects.

C. Source Drift As will be understood by those having ordinary skill in the -art, variations, or drift, in the infrared source may also cause drift in the output signals of the thermopile detectors 12, 14, 22, 24, 32 and 34 illustrated in FIG. 2. This drift may be eliminated by using two analytical filters, a first having its transmission at the absorption wavelength of the gas being analyzed, and a second designed to transmit some other unabsorbed wavelength. Energy in the unabsorbed band serves as a reference.
This technique of referencing is well-known and -is described in textbooks, see, e.g., Mullard Limited, A~lications of Infrared Detectors. ISBN # 901232 22X, Chapter lO, the pertinent portions of which are incorporated by reference as if fully set forth herein.

D. Optically Stabilized Gas Analyzer A typical construction of a preferred embodiment of the present invention is illustrated in FIG. 2. The circuitry and other components which comprise the present invention will generally be assembled into a housing 50, appropriately -~

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~6 4~9 22 PCT/US90/04875 configured to enable the various components to function as described below. Those of ordinary skill will be aware of the design parameters associated with the packaging of devices made in accordance with the present invention. Some of the considerations relevant to the design of the housing 50 are:
external interface design, cooling requirements, shielding and isolation characteristics, size and weight, integration with a breathing tube, sample cell or other means of delivering a sample of the patient's expired air, and aesthetic and utility considerations.
An input signal 80 from a host processor or other source is transmitted through an analog hybrid 42, the signal from which excites a source of infrared radiation 40. A reflector 52 is provided to efficiently direct an incident beam of infrared radiation. The incident radiation passes through an optical window 54 and into the region of the gas stream to be analyzed 58. The gas stream itself may be contained in apparatus such as a clear tube or tube-liXe structure (not shown), which directs a portion of the gaseous flow through the measurement region 58.
After the incident infrared radiation has passed through the gas stream, it will pass through another optical window S6, bandpass filters 60, 61 and 62 and neutral density attenuation filters 16, 18, 26, 28, 36 and 38 before finally reaching the thermopile d-t-ctors 12, 14, 22, 24, 32 and 34.
The embodiment pictured in FIG. 2 is designed to measure the conc-ntration of two gases and may be denominated a three-channel d t-ctor, with one channel serving as a reference channel. As will be appreciated by those of ordinary sXill, detectors may be : . ,- ,,, -~ . ~" -~ ' ' '' "" .
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wosl/03204 PCT/US90/048~5 23 2 0 6~ 8 92 ~~
constructed having anywhere from one to many channels, depending upon the number of constituent gases to be detected and analyzed.
Thus, for example, in FIG. 2 in addition to detectors 12 and 14, second and third detector assemblies 22 and 24 and 32 and 34 are used to create three channels. Positioned above each detector assembly is a bandpass filter 60, 61 and 62, each channel employing a different bandpass filter. Thus, it is understood that a first channel comprises detectors 12 and 14, attenuation filters 16 and la, and bandpass filter 60. A second channel comprises detectors 22 and 24, attenuation filters 26 and 28 and bandpass filter 61, and so forth.
The output signal for each channel, i.e., the difference signal described above, is passed through its respective amplifier 20 and transmitted to a multiplexer 44, which also receives a signal from a tem~erature sensor 41. The multiplexer 44 then outputs a detector signal 45, which is also combined with a signal from an electronically erasable programmable read only memory (EEPROM) device 46 to fashion an output signal 90. The Seebeck coefficient, described above, is stored in the EEPROM 46, and is used for scaling the detector signal 45 to indicate absolute gas concentration values.
Attenuation filters 16, 18, 26, 28, 36 and 38 are mounted dir-ctly on the ceramic substrate. Therefore, the output of the temperature sensor 41 will reflect the temperature of the attenuation filters as well ag the reference junction temperature of the thermodetectors. A heater 30 is also shown which may further regulate the temperature of the apparatus, if desired.

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~ 24 E. Bandpass Filters The bandpass filters 60, 61 and 62 are placed an equal distance in front of their associatet detectors, i.e., they are placed in a common plane, so that all three thermopile detectors 5 have an equal field of view. Each filter is characterized by its center wavelength and half-power bandwidth. The conventional approach to specifying the bandpass filters would be to center the filters in the absorption band of interest and to make the bandwidth as wide as the absorption band. The present invention 10 takes a different approach, however, than that of the prior art and utilizes bandpass filters having center wavelengths shifted away from the center of the absorption band and bandwidths wider than the absorption band. The method of specifying the bandpass filters in accordance with the present invention is described in 15 more detail in the following section. The shifting and broadening of the bandpass filter minimizes cross-talk between channels and minimizes the effects of temperature variations and manufacturing tolerances on the filters.
For example, in a preferred embodiment of the invention one 20 channel is used to detect CO2, another channel is used to detect N2O, and a third channel is used as a reference channel. The ab~orption band o~ CO2 is centered at 4.256 microns, and the h~lf-pow-r wavelength is 0.180 microns. In a preferred e~bodiment of the present invention, however, the bandpass filter 25 u~-d for the CO2 channel is centered at 4.2624 microns with a half-power bandwidth of 0.2088 microns. Due to manufacturing to~erances, the half-power wavelengths may vary by plus or minus ~ - - -- - . . . , , - . ~ . .

, , , . - -~ -': . .. . . . .
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. '~ :. ':-. .. , .-- - -~, ~ . - .- . . . - - - -~ - --WO91/0320~ PCT/US90/04875 25 206489~
0.03 microns at the short wavelength edge, and plus 0.03 microns to minus 0.05 microns at the long wavelength edge.
The absorption band for N20 is centered at 4.5400 microns, with a bandwidth of 0.3 microns. For the reasons stated above, -in a preferred embodiment the bandpass filter for the N20 channel has a center wavelength of 4.5397 microns and a bandwidth of 0.3190 microns. The short wavelength half-power point may by plus O.Ol microns to minus 0.03 microns. The lo~g wavelength half-power point varies by plus or minus 0.03 microns.
The reference filter has a center wavelength of 4.8265 microns and a half-power bandwidth of 0.2088 microns. The short and long bandwidth edges may vary by plus or minus 0.03 microns. ~ -The bandwidth is designed to be as close as possible to the -bandwidth of the C02 filter. This minimizes the thermal gradients across the substrate since the total energy passing through this filter will approximate the total energy passed by the C2 filter. The center wavelength is selected to be as close -~
as possible to the center of the C02 and N20 bands, while at the .ir~ 3.
same time maintaining isolation between those channels and the reference channel. Thus, this novel use of band shifting and widening, to minimize cross-tal~ and the effects of thermal shift and manufacturing tolerances, in the design of the bandpass filt-rs 60, 61 and 62 i8 integral to carrying out the preferred mbodiment.
1. Analytical ~andpass Filter Specification This section describes a method for specifying bandpass filters for a preferred embodiment of an optically stabilized capnograph in accordance with the present invention. The ... . . .. . .. .
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-WOgl/03204 ~9~ 26 PCT/US90/04875 following example describes the specification of bandpass filters employed by the CO2, NO2 and reference channels of a three channel analyzer. The method described does not deal with the construction of filters, but rather with a novel method of 5 specifying bandpass filters for use in infrared gas analyzers, or capnographs.
: a. Conventional Technique From the prior art, a technique for specification of infrared bandpass filters can be summarized. The guidelines, or 10 steps, can be stated as:
1) Specify a filter that has its center wavelength coinciding with the center wavelength of the gas intended to be analyzed. This is done to yield maximum specificity and minimum cross.-talk.
2) Specify the half power bandwidth just wide enough to include all of the wavelengths absorbed by the gas of interest. This optimizes modulation, or the amount of energy, passed by the filter and absorbed by the gas. ~ -In practice it is understood that filter center wavelengths 20 change with temperature. This is shown at page 41 of the OCLI
Infrared Handbook (1970) Optical Coating Laboratory Inc.
In the construction of gas analyzers incorporating filter de~ign~ engineers often overcome the filter shift by operating the Silters in a temperature controlled environment. Such a 25 design is taught by U.S. patent No. 4,423,739 to Passaro. This approach, however, is expensive and complicated. It is also recognized that manufacturing tolerances on infrared bandpass filters can result in a range of center wavelengths from a single .,_ 7,~
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production run. This is expressed as a +/- tolerance of -typically 1/2% to 1% on the center wavelength. Accommodating this variation is often accomplished by calibrating each analyzer individually. This practice is also expensive.
In specifying CO2 and NO2 filters in accordance with the present invention, the first two steps consist of steps 1 and 2 of the conventional technique; i.e., conventional filters are specified. In the present example, gas spectra from SADTLER
INDEX were used.
The resulting conventional filters are characterized by the following filter specifications, titled VER 1.2. They follow in written form and a graph which shows the filters as specified and as shifted by +.03u, which is approximately 0.7%. It corresponds to the shift that would be produced by a rise in temperature of ~if~
about 50- C. It also corresponds to the manufacturing tolerance specified. For reference, the spectra of CO2 and NO2 are also included on the graphs.
b. Analysis and Computer Performance Simulation ~ .
Following the drafting of the VER 1.2 specifications, a computer simulation technique was developed to test the validity of the design. A Perkin Elmer 1640 FTIR spectro-photometer (PE 1640) was used to measure the absorption spectra Or the gases of interest, CO2 and N20. The gases were at atmospheric pressure and in a 0.5 inch path length cell. 5.0%
C2 and 50% N2O balance 2 were used. The spectra data were trans~erred into a personal computer, with data reported every O.1U. These spectra were combined in a spreadsheet program with mathematical models of the filters. Modulation percentages were ~ '; . :.
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wogl/03204 Q6 ~92 PCT/US90/04875 calculated by multiplying the gas spectra by the rilter models and dividing the result by the product of the spectra and a 100%
transmission model Modulation, cross-talk, and erfects of filter shifts were studied The results of this analysis will be discussed below in the section on performance comparison The analysis showed that in order to meet the design goals of the project either individual calibration or temperature control of the filters, or both, would have to be specified It was decided to optimize the filter specifications to avoid these complications c Optimal Filter Specification Next, the conventional filters were optimized by the following three steps 3) ~he filter center wavelength was varied so as to minimize the modulation change as the filter shifts over 0 3u 4) The filter center wavelength and bandwidth were varied to minimize cross-talk 5) The filter center wavelength and bandwidth were varied to ~inimize the change in cross-talk that occurred due to the filter shifting 0 3u To provide a realistic shape to the simulated bandpass filter, the transmi~sion of a real infrared bandpass filter was a~ur-d with the PE 1640 A data file was created which pr-~-rv-d the cut-on and cutoff edges of the real filter but r-placed the middle section with a flat transmission of 80% A
progr~m changed the width o~ the simulated filter by altering the width of the flat top to allow testing various filter bandwidths The si~ulated rilter was restricted to half-power bandwidths of ,:

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.- -wosl/o32o4 ~ , PCT/US90/04875 29 20~4892 greater than O.lu to insure that the resulting optimized filter was manufacturable. With the gas spectra in memory and the adjustable ideal filter file prepared, a personal computer was programmed to sweep through all possible filter combinations for CO2 and N20 filters and to select the best combination as indicated by:
1) Maximum modulation;
2) Minimum modulation change over 0.3u filter shift, 3) Cross-talk modulation less than 0.7~ for CO2 (apx. 1 mmHg); and 4) Cross-talk modulation less than 1.0% for N2O -(about 10 mmHg).
d. Performance and comparison of VER 1.2 and VER 2.1 :.
Filters (iJ Modulation The optimized filter VER 2.1 ~as slightly less modulation than the conventional version.

VER 1.2 VER 2.1 5% CO2 40.3% 36.0% MODULATION

50% N2O 6S.4% 5B.9% MODULAT}ON

This is due to the fact that both the VER 2.1 C2 and N20 -filters are slightly narrower than the conventional VER 1.2 filters and not centered on the center of absorption for CO2 and N2O, respectiVely. This reduction is of little or no significance in the overall design of the analyzer.

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?,~ 6 ~ Pcr/uS9~/~875 (ii) Filter shift Error The sacrifice in modulation was orfset by a much improved performance with respect to errors when the filters shift.

VER 1.2 NORMAL SHIFTED CHANGE CHANGE
~ MOD %MOD % MOD mmHg co2 CHANNEL
5% CO240.3 41.5 1.2 1.7 50% N20 0.2 0.3 0.1 0.1 ,~ i-i~

5% CO20.8 0.7 -0.1 -1.0 :
50% N2O 6S.4 54.2 -11.2 -112.0 .-VER 2.1 NORMAL SHIFTED CHANGE CHANGE
% MOD %MOD % MOD mmHg ~-5% CO236.0 36.3 0.3 0.4 50% N2O0.4 0.5 o.i 0.1 8 5% CO21.0 0.8 -0.2 -2.0 ~ -~
50% N2O58.9 56.3 -2.6 -26.0 The optimized filter specification reduced CO2 error due to .
a shift of 0.3u reduced from 1.7 mmHg to 0.4 and the N20 error ~.
went from 112 to 26 mmHg.
(ii~J Cross-t~lk Cross-talk increased slightly from VER 1.2 to VER 2.1.
3S `.
CROSS-TALK E M OR `
VER 1.2 VER 2.1 %MOD mmHg%MOD ~mHq S0% N,O 0.2 0.3 0.4 0.6 S% CO2 0.8 8.0 1.0 10.0 , ,., , . . : .. - -.. , ~ -. ~ - . . :.' - :-:~ . .:~. . - .. .. .. .. : ... ~ :; :

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wosl/o32o4 PCT/US90/04875 206~892 e. Sum~ary The method yielded a filter set which is slightly different from that selected ~y conventional methods and, according to the simulations, better suited to yield a manufacturable gas analyzer with Iittle or no individual adjustment. Preferred filter specifications are set forth in Table ~ below:
TAB~F I
INFRARED FILTER SPECIFICATIONS

ALL FILTERS:
Dimensions: 0.187" X 0.156" ,+1- .003"
0.020", +1- .001" thick 15 Edge Irregularities: <0.005"
Temperature Shift: 0.01% per Deg. C.
Angle Shift: 0.001% per Degree of angle. -Transmission at Center: 80%
Cut-on - Cutoff Slopes: 3 Humidity Withstand per MIL-C-675A
Abrasion Withstand per MIL-C-675A
Coating Adherence per MIL-M-13508B

Spectral Characteristics below apply at 0 Deg.
incidence and 30 Deg. C. -FILTER 1: Center 4.255 micron +/- 0.03 micron -Half Power Bandwidth 0.180 micron +/- 1%

30 FILTER 2: Center 4.540 micron +/- 0.05 micron ~alf Power bandwidth 0.300 micron +/- 1%

FI~OEER 3: Center 3.600 micron +/- 0.03 micron Half Power Bandwidth 0.180 micron +/- 1 F. Optically Stabilized Gas Analyzer Used With A ~ost Processor In FlG. 3 i8 illustrated a preferred embodiment of certain ~ignal processing circuitry 100 used to carry out the present invention in conjunction with a host system. The input and output signals to the detector apparatus 80 and 90 are passed through an isolation and filtering subsystem 140 to insure patient safety. Output signal 90 of the detector flows through tbe isolation subsystem 140 to the AD converter detector 130, . .' ' .

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~:' ' ' . ' ' ' _ WO91/03204 ~ ~ 4~9~ PCT/US90/04875 where it is digitized, before input into the microprocessor 120.
Finally, the microprocessor 120 transmits the processed detector output -- as a concentration value for the respective constituent gas -- to the host system interface llo, and on to the host system (not shown). The final output signal may be monitored, recorded, stored, or further manipulated. Alternatively, a signal from the host system to the detector apparatus shown in FIG. 2 may be transmitted to the host system interface 110, then to the microprocessor 120, through the isolation and filtering subsystem 140, and finally on to the input 80 of the detector apparatus. The signal from the host system is not converted from digital to analog form before being input to the detector apparatus.
Although certain preferred embodiments of the present invention have been described herein, it should be understood that the invention is not so limited. For example, FIG. 8 illustrates a schematic representation of an alternate portion of a detector in accordance with the invention. As explained above with reference to FIG. 4, the emission from a source of infrared radiation 300 falls upon the detector 202. However, in the embodiment of FIG. 8, the functions of the neutral density and analytical filters described above are combined into the same element. Specifically, a first filter 260 having a tran~mi~sivity of 100% and a second filter 262 having a tran~mi~sivity of 50% are provided. The remainder of the detector 202 is the same as that described above with reference to FIG. 4, i.e., an aperture or window 230, detectors 216 and 220 and processor 240 are again provided. The reference portion of : ..~ - . .

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WO9l/03204 PCT/US90/04875 20~i892 -the circuit may either be constructed as shown in FIG. 4, or using a pair of 50%/100% filters, as shown in FIG. 8. Thus, the analytical filters may be functionally combined with the neutral density filter as one filter element.
Although certain preferred embodiments of the present invention have been described herein, it should be understood that the invention is not so limited. Thus, many variations of the specific embodiments heretofore described are within the scope of the present invention as defined by the following claims.

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Claims (28)

What is claimed is:
1. A device for detecting the concentration of constituents of the respiratory airstream of a patient, comprising:
(a) a source of infrared radiation;
(b) a pair of physically separate infrared detectors for each constituent whose concentration is to be determined, said detectors being disposed on the same substrate so as to receive incident radiation from said infrared radiation source and to produce electrical signals representative of the received incident radiation;
(c) means for directing at least a portion of said respiratory airstream of said patient between said detectors and said infrared radiation source;
(d) attenuating means, disposed between only one of said detectors in each pair and said directing means, for attenuating the incident radiation impinging upon only said one detector in each pair; and (e) means for processing said electrical signals representative of the incident radiation received at each pair of detectors so as to produce optically stabilized signals substantially unaffected by changes in the ambient temperature of the environment in which said device operates.
2. The device of claim 1, further comprising a pair of physically separate reference infrared detectors disposed on said substrate so as to receive incident radiation from said infrared radiation source which has passed through said respiratory airstream and to produce electrical signals representative of the received incident radiation, whereby said attenuating means is disposed between only one of said reference detectors and said directing means for attenuating the incident radiation impinging upon only said one reference detector.
3. The device of claim 2, further comprising optical filters disposed between each said pair of infrared detectors and said directing means and an optical filter disposed between said pair of reference infrared detectors and said directing means, said optical filters passing a narrow band of energy about a wavelength readily absorbed by the constituent of the respiratory airstream of which its concentration is to be measured by a corresponding pair of detectors and said optical filter passing a band of energy excluding said wavelengths readily absorbed by said constituents of the respiratory airstream of which their concentrations are to be determined.
4. The device of claim 3, wherein said processing means comprises means for determining first differences between electrical signals produced by respective pairs of infrared detectors and a second difference between electrical signals produced by said pair of reference infrared detectors, means for determining respective ratios between said first differences and said second difference, and means for computing from said ratios the concentrations of the constituents of the respiratory airstream whose concentrations are to be determined.
5. The device of claim 1, wherein said constituents are carbon dioxide and nitrous oxide.
6. The device of claim 1, further comprising a housing having first and second optical windows constructed to permit the respective transmission of infrared radiation from said source through said first optical window, through said directing means, through said second optical window, and thereafter through said attenuating means before impinging upon each of said pairs of infrared detectors.
7. The device of claim 1, further comprising an external processing system and an interface for interfacing inputs from said external processing system to said source so as to activate said source and for interfacing outputs of said processing means to said external processing system for further processing.
8. The device of claim 7, wherein said interface comprises a filter for isolating said external processing system from said patient, an analog to digital converter for digitizing analog inputs from said external processing system, and a microprocessor for determining concentration values for said constituents from said optically stabilized signals.
9. The device of claim 1, wherein said attenuating means comprises an optical filter with a transmission coefficient of approximately 0.50.
10. The device of claim 1, wherein said pair of infrared detectors comprises a pair of thermopiles in opposed relation to each other.
11. A shutterless infrared capnograph for detecting the concentration of constituents of the respiratory airstream of a patient, comprising:
(a) a source of infrared radiation;
(b) a pair of physically separate infrared detectors disposed on the same substrate so as to receive incident radiation from said infrared radiation source which has passed through said respiratory airstream and to produce electrical signals representative of the received incident radiation;
(c) a pair of physically separate reference infrared detectors disposed on said substrate so as to receive incident radiation from said infrared radiation source which has passed through said respiratory airstream and to produce electrical signals representative of the received incident radiation;
(d) means for directing at least a portion of said respiratory airstream of said patient between said detectors and said infrared radiation source:
(e) attenuating means, disposed between only one of said detectors and said directing means and between only one of said reference detectors and said directing means, for attenuating the incident radiation impinging upon only said one detector and upon said one reference detector;
(f) a first optical filter disposed between said pair of infrared detectors and said directing means for passing a narrow band of energy about a wavelength readily absorbed by a constituent of the respiratory airstream of which its concentration is to be determined;
(g) a second optical filter disposed between said pair of reference infrared detectors and said directing means for passing a band of energy excluding said wavelength readily absorbed by a constituent of the respiratory airstream of which its concentration is to be determined; and (h) means for processing said electrical signals representative of the received incident radiation so as to produce an optically stabilized signal substantially unaffected by changes in the ambient temperature of the environment in which said device operates, said processing means comprising means for determining the difference between electrical signals produced by said pair of infrared detectors and the difference between electrical signals produced by said pair of reference infrared detectors, means for determining a ratio between said differences, and means for computing from said ratio the concentration of the constituent of the respiratory airstream whose concentration is to be determined.
12. A method of detecting the concentration of a gaseous component of a substantially gaseous flow stream, comprising the steps of:
transmitting a beam of infrared radiation through said substantially gaseous flow stream;
attenuating a portion of said infrared radiation which has passed through said substantially gaseous flow stream;

detecting the intensity of said infrared radiation using a first detector and generating a first signal;
detecting the intensity of only said attenuated portion of said infrared radiation using a second detector, physically separate from said first detector and disposed on the same substrate as said first detector, and generating a second signal;
computing the difference between said first signal and said second signal and generating a difference signal; and processing said difference signal to produce an optically stabilized signal representative of the concentration of said gaseous component, whereby temperature gradients between said first and second detectors are prevented such that said optically stabilized signal is substantially unaffected by changes in the ambient temperature of the environment.
13. The method of claim 12, comprising the further step of filtering said infrared radiation and said attenuated portion of said infrared radiation through an optical filter which passes a narrow band of energy about a wavelength readily absorbed by said gaseous component of a substantially gaseous flow stream.
14. The method of claim 13, comprising the further steps of:
filtering said infrared radiation and said attenuated portion of said infrared radiation through a blocking optical filter which passes a band of energy excluding said wavelength readily absorbed by said gaseous component of said substantially gaseous flow stream;

detecting the intensity of the infrared radiation filtered by said blocking optical filter using a third detector disposed on said substrate and generating a third signal;
detecting the intensity of the attenuated portion of the infrared radiation filtered by said blocking optical filter using a fourth detector, physically separate from said third detector and disposed on said substrate, and generating a fourth signal;
computing the difference between said third signal and said fourth signal and generating another difference signal; and processing said difference signal with said another difference signal to determine said concentration of said gaseous component of said substantially gaseous flow stream.
15. The method of claim 14, wherein said step of processing said difference signals comprises the step of determining a ratio between said difference signal and said another difference signal.
16. A method of monitoring the respiratory condition of a patient, comprising the steps of:
transmitting a beam of infrared radiation through a respiratory airstream of said patient;
attenuating a portion of said infrared radiation which has passed through said respiratory airstream;
filtering said infrared radiation and said attenuated infrared radiation through an optical filter which passes a narrow band of energy about a wavelength readily absorbed by a constituent of said respiratory airstream indicative of the respiratory condition of the patient;
detecting the intensity of said filtered infrared radiation using a first detector and generating a first signal;
detecting the intensity of only said filtered and attenuated infrared radiation using a second detector, physically separate from said first detector and disposed on the same substrate as said first detector, and generating a second signal;
computing the difference between said first signal and said second signal and generating a difference signal;
processing said difference signal to determine a concentration of said constituent of said respiratory airstream of the patient substantially independent of changes in the ambient temperature of the environment; and monitoring the concentration of said constituent of said respiratory airstream of the patient as an indicator of the respiratory condition of the patient.
17. A method of selecting an optical filter for use in a respiratory gas analyzer which measures the concentration of a predetermined respiratory gas constituent, comprising the steps of:
selecting a nominal center wavelength for said optical filter which coincides with a center wavelength readily absorbed by said constituent;
selecting a half-power bandwidth just wide enough to pass substantially all of the wavelengths absorbed by said constituent;

varying said nominal filter center wavelength so as to minimize modulation change as said optical filter is shifted over a predefined range of wavelengths;
varying said nominal filter center wavelength and its bandwidth so as to minimize cross-talk between said said constituent and other constituents: and varying said nominal filter center wavelength and its bandwidth so as to minimize changes in cross-talk as said optical filter is shifted over said predefined range of wavelengths.
18. An infrared energy detector for measuring the amount of incident radiation received from a source of infrared energy, comprising:
first and second thermopiles, positioned on the same substrate so as to receive incident infrared energy from said infrared energy source, for producing output electrical signals representative of the intensity of said incident infrared energy;
and means for distinguishing desired infrared energy signal components of said incident infrared energy from undesired thermal effects, comprising:
a first optical path between said infrared energy source and said first thermopile, said first optical path including an analytical filter chosen to selectively pass an infrared wavelength of a desired infrared energy signal component, a second optical path between said infrared energy source and said second thermopile, said second optical path also including said analytical filter chosen to selectively pass the infrared wavelength of the desired infrared energy signal component, and an attenuating neutral density filter located in only one of said first and second optical paths.
19. The infrared energy detector of claim 18, further comprising means for determining a differential signal from output signals produced by said first and second thermopiles.
20. The infrared energy detector of claim 18, further comprising:
third and fourth thermopiles, positioned on said substrate so as to receive incident infrared energy from said infrared energy source, for producing output electrical signals representative of the intensity of said incident infrared energy, wherein said means for distinguishing desired infrared energy signal components of said incident infrared energy from undesired thermal effects further comprises:
a third optical path between said infrared energy source and said third thermopile, said third optical path including an analytical filter chosen to selectively block the infrared wavelength of the desired infrared energy signal component, a fourth optical path between said infrared energy source and said fourth thermopile, said fourth optical path also including said analytical filter chosen to selectively block the infrared wavelength of the desired infrared energy signal component, and said attenuating neutral density filter is further located in only one of said third and fourth optical paths.
21. The infrared energy detector of claim 20, further comprising means for determining a first differential signal from the output signals produced by said first and second thermopiles and a second differential signal from the output signals produced by said third and fourth thermopiles.
22. The infrared energy detector of claim 21, further comprising means for forming a ratio of said first and second differential signals.
23. The infrared energy detector of claim 18, wherein said analytical filter chosen to selectively pass the infrared wavelength of the desired infrared energy signal component and said attenuating neutral density filter are combined into a single filter element.
24. The infrared energy detector of claim 18, wherein said attenuating neutral density filter has a transmission coefficient of approximately 0.50.
25. The infrared energy detector of claim 18, wherein said attenuating neutral density filter has a transmission coefficient of approximately 0.
26. The infrared energy detector of claim 18, wherein said first and second thermopiles are connected in opposed relation to each other.
27. The device of claim 1, wherein said substrate is a ceramic substrate and said pair of infrared detectors are disposed on physically separate portions of said substrate.
28. The device of claim 11, wherein said substrate is a ceramic substrate and said pair of infrared detectors and said pair of reference infrared detectors are disposed on physically separate portions of said substrate.
CA002064892A 1989-09-01 1990-08-27 Shutterless optically stabilized capnograph Abandoned CA2064892A1 (en)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US40195289A 1989-09-01 1989-09-01
US401,952 1989-09-01
US07/522,177 US5081998A (en) 1989-09-01 1990-05-11 Optically stabilized infrared energy detector
US07/522,208 US5095913A (en) 1989-09-01 1990-05-11 Shutterless optically stabilized capnograph
US522,177 1990-05-11
US522,208 1990-05-11
PCT/US1990/004875 WO1991003204A1 (en) 1989-09-01 1990-08-27 Shutterless optically stabilized capnograph

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JP (1) JPH05500112A (en)
AU (2) AU637827B2 (en)
CA (1) CA2064892A1 (en)
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AU4430593A (en) 1993-10-14
GR1001000B (en) 1993-03-31
AU637827B2 (en) 1993-06-10
GR900100645A (en) 1992-01-20
PT95178A (en) 1992-05-29
EP0489840A1 (en) 1992-06-17
EP0489840A4 (en) 1992-08-12
JPH05500112A (en) 1993-01-14
WO1991003204A1 (en) 1991-03-21

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