WO1991009372A1 - Analyse assistee par ordinateur du sommeil - Google Patents

Analyse assistee par ordinateur du sommeil Download PDF

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Publication number
WO1991009372A1
WO1991009372A1 PCT/US1990/007189 US9007189W WO9109372A1 WO 1991009372 A1 WO1991009372 A1 WO 1991009372A1 US 9007189 W US9007189 W US 9007189W WO 9109372 A1 WO9109372 A1 WO 9109372A1
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WIPO (PCT)
Prior art keywords
recorded
physiological signals
scoring
display
parameters
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PCT/US1990/007189
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English (en)
Inventor
Ivan Pal
Gil Raviv
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Bio-Logic Systems Corporation
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Application filed by Bio-Logic Systems Corporation filed Critical Bio-Logic Systems Corporation
Publication of WO1991009372A1 publication Critical patent/WO1991009372A1/fr

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/72Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7235Details of waveform analysis
    • A61B5/7264Classification of physiological signals or data, e.g. using neural networks, statistical classifiers, expert systems or fuzzy systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/24Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/316Modalities, i.e. specific diagnostic methods
    • A61B5/369Electroencephalography [EEG]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/72Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7235Details of waveform analysis
    • A61B5/7264Classification of physiological signals or data, e.g. using neural networks, statistical classifiers, expert systems or fuzzy systems
    • A61B5/7267Classification of physiological signals or data, e.g. using neural networks, statistical classifiers, expert systems or fuzzy systems involving training the classification device
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H50/00ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/20ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems

Definitions

  • the present invention relates generally to computer assisted analysis of physiological data and, more particularly, to computer assisted analysis of sleep.
  • disorders in sleeping and in a ing-up has been recognized for centuries. Accordingly, various disorders are now well recognized and a classification system for such disorders was adopted in 1979.
  • This classification system recognizes distinct disorders in initiating and maintaining sleep (insomnias), in excessive somnolence, in the sleep-wake schedule, and dysfunctions associated with sleep, sleep stages, or partial arousals (parasomnias) . Included among the preceding major categories of disorders and dysfunctions are various syndromes such as sleepwalking, nightmares, sleep related asthma, sleep apnea, alveolar hypoventilation, narcolepsy, and epilepsy related to stages of sleep.
  • EKG electro-cardiac
  • respiration signal respiration signal
  • blood oxygen saturation signal Sa02
  • other signals may also be recorded throughout the night. Subsequently, this data is summarized for successive short intervals of time during the night, typically 30 seconds in length although intervals having different durations such as 20 seconds or 60 seconds may be used. During each of these successive intervals, which are called “epochs,” the recorded physiological data is analyzed to assign each epoch to one of the seven different categories of sleep established in the Rechtschaffen and Kales scoring system.
  • the physiological data for an entire night has been recorded using a multi-channel ink-on-paper strip chart recorder. This record is then manually analyzed to score the various stages of sleep. Because certain signals such as the EEG have significant components with frequencies as high as 90 Hz, the recording paper generally passes through the chart recorder at a linear velocity of 10 to 20 mm/sec. Consequently, using this multichannel recording technique, the data for a single night's sleep is extremely bulky and occupies several thousand pages of recording paper. Obviously, the manual summarization of the data recorded on this volume of paper is time " consuming, clumsy and awkward, particularly if it is desirable to juxtapose and compare the data for two different epochs of sleep that are widely separated in time.
  • the traditional recording technique for analyzing sleep data is poorly adapted to recording and analyzing snoring.
  • the audible signals that occur during snoring contain significant information in frequencies extending up to several kilohertz. However, such audible frequencies are 500 to 1,000 times higher than the maximum frequency of the EEG signals recorded during sleep.
  • audible signals associated with snoring were recorded directly onto a strip chart, the number of pages recorded during a night would increase by 500 to 1,000 times over that presently being recorded.
  • the envelope of the audible signals associated with snoring were recorded directly on to a strip chart, the number of pages recorded during a night would increase by 50 to 100 times over that presently being recorded.
  • the low frequency wave is characterized by the time difference between successive zero crossings and by the amplitude difference between consecutive peaks. If the equivalent frequency of a low frequency wave lies outside the range of 0.5 to 6 Hz, it is rejected.
  • Various parameters controlling this analysis may be changed from a computer console and the results of the waveform analysis are displayed graphically.
  • PCT Patent Cooperation Treaty
  • feature extraction depends upon the particular signal being analyzed and employs various parameters such as amplitude, frequency, time of occurrence and duration.
  • Features are extracted in real time for each successive 30 second epoch throughout the night.
  • samples of the unprocessed data are also stored in long term computer storage at a resolution selected to allow reclassification of the data if that is required.
  • the frequency analysis portion of feature extraction is performed using adaptive Fourier analysis for the EOG and EMG signals, and for five mutually exclusive frequency bands in the EEG signal.
  • Pattern detection for the EEG, EOG and EMG signals consists in identifying "transient pattern candidates" in each of those signals that satisfy, four different categories of detection criteria.
  • the first category of detection criteria employs the extracted features to identify transient pattern candidates in individual signals.
  • the second category of detection criteria involve the synchronism or lack thereof between a particular transient pattern candidate in one signal and concurrent events in other signals.
  • the third category of detection criteria involve the context in which a particular transient pattern candidate occurs in terms of its relationship with other types of patterns or measured variables.
  • the fourth category of detection criteria identify patterns as a combination of other, previously identified patterns.
  • the computer system disclosed in this PCT patent application scores successive 30 second epochs of sleep into six classes — awake, rapid eye movement ⁇ "REM" sleep, and sleep stages I - IV. Classification is performed by checking whether the EEG, EOG and EMG patterns in each epoch fulfill the criteria that identify one of the 6 classes of sleep. If the criteria for all of the six classes are unsatisfied, the epoch is designated as undefined.
  • the parameters used in performing each of the three preceding steps may be taken from a "Knowledge Base,” and may be interactively changed by the operator prior to initial processing and/or reclassification.
  • an operator may graphically change threshold levels and/or disable or activate classification rules.
  • the systems graphically displays sleep scoring results for an entire night, and permits interactive enlargement of the signals for selected short intervals at any time throughout the night. Also various stages of sleep may be selected interactively for which mean values of the stages are then calculated from the recorded data. An operator may then use these results in interactively changing the processing parameters before rescoring the data.
  • the present invention provides an improved apparatus for recording physiological data throughout a night's sleep and for analyzing that data after it has been recorded.
  • An object of the present invention is to provide an apparatus that facilitates quickly analyzing physiological data recorded throughout a night's sleep.
  • Another object of the present invention is to provide an apparatus that increases the accuracy of sleep scoring.
  • Another object of the present invention is to provide an apparatus that permits easily and conveniently changing among various different displays of the results of sleep analysis.
  • Another object of the present invention is to provide an apparatus that simultaneously displays ' different types of physiological data recorded throughout a night's sleep at differing time scales.
  • Another object of the present invention is to provide an apparatus that provides a library for storing protocols for sleep scoring.
  • Another object of the present invention is to provide an apparatus that may record and analyze audible events that occur during sleep.
  • Yet another object of the present invention is to provide an apparatus for the scoring of sleep which is both simple and cost effective, and which facilitates the scoring of sleep.
  • the apparatus of the present invention includes a computer system specially adapted to assist an operator in analyzing sleep and in scoring the stages of sleep that occur throughout an entire night.
  • the operator first identifies the several physiological signals for which data is recorded. After the physiological signals have been identified, the operator then selects among various different formats for graphically displaying the recorded data. Having selected a display format, the operator then establishes a set of parameters that identifies a specific waveform in the physiological signals that characterize a particular type event in the recorded data.
  • the computer scores events occurring throughout the night's sleep by applying these parameters, i.e. a data analysis protocol, to the recorded data.
  • the computer then provides a graphic display of the scoring results for the operator's review and possible re-scoring using a different protocol.
  • the operator establishes the protocol, by first selecting a set of initial values for disting ⁇ uishing events in the recorded data. This initial protocol is then used to identify events in a portion of the recorded data and the results of this trial event identification are displayed for the operator's review. In reviewing this trial identification, the operator classifies the events into those that have been identified correctly and those that have been identified incorrectly. Using this event classification, the computer then adjusts the parameters to conform with the correctly identified events. These adjusted parameters are then applied to the recorded data in scoring the night's sleep. Thus, an operator may interactively "teach" the computer the particular way in which a subject's sleep is to be scored.
  • the operator enters selected physical characteristics about a subject, e.g. the subject's age, sex, etc. These physical characteristics are then used to retrieve an initial protocol from a library of previously recorded protocols. Data recorded for the physiological signals is then scored using this initial protocol after which a second protocol, to be used in scoring the night's sleep, is then retrieved from the protocol library based upon the results of scoring with the initial protocol.
  • the various display formats provided by the computer program allow an operator to review the computer program's sleep analysis in numerous different ways. These various display formats allow displaying a summary of the scoring of successive 30 second epochs of sleep into eight different classes — movement time, waking state, REM sleep, sleep stages I - IV or arousal. The formats also allow displaying hypopnea and apnea events and whether such events were central, obstructive, or mixed.
  • FIG. 1 is a block diagram depicting a digital computer system for use in the collecting and analyzing sleep data when executing a sleep analysis computer program;
  • FIG. 2 is a block diagram depicting the hierarchy of menus provided for controlling the operation of the sleep analysis computer program;
  • FIG. 3 illustrates graphical display of a single thirty second epoch of several different physiological signals in a polygraph display format;
  • FIG. 4 illustrates graphical display of several different physiological signals in a staging display format which enlarges a single epoch of different physiological signals, such as might be displayed in FIG. 3, into three contiguous 10 second intervals;
  • FIG. 5 illustrates graphical display of several different physiological signals in a respiratory display format which displays four physiological signals particularly relevant to analyzing respiratory disturbances
  • FIG. 6 illustrates a respiratory disturbance log superimposed over the respiratory display format depicted in FIG. 5;
  • FIG. 7 illustrates a graphical display of the same physiolog ⁇ ical signals during different epochs in the recorded data
  • FIG. 8 illustrates the parameters used in automatic scoring of sleep staging
  • FIG. 9 illustrates the hypnogram display format for displaying the results of sleep scoring
  • FIG. 10 illustrates the summary display format for displaying the results of sleep scoring and respiratory analysis
  • FIG. 11 illustrates a graphical display of different physiological signals with differing time intervals over which the various signals are displayed
  • FIG. 12 illustrates a graphical display of two different physiological signals, each being displayed with different durations of data.
  • FIG. 1 depicts a digital computer system in accordance with the present invention, identified by the general reference character 30.
  • the digital computer system 30, which includes a microcomputer based digital computer 32, is connected to either an EEG machine or polysomnograph 34 to adapt it for collecting and analyzing sleep data.
  • the digital computer 32 is preferably an IBM/AT compatible microcomputer that includes either an 80386 or 80268 microprocessor 35 that respectively runs at a clock speed of 20 MHz or 16 MHz.
  • Electrodes and other sensors 36 are connected, in a conventional manner, from the EEG machine or polysomnograph 34 to obtain physiological signals from a subject 38 whose sleep is to be scored.
  • a pair of EEG electrodes 36 are attached to the subject 38 to provide a A1-C4 EEG signal to the EEG machine or polysomnograph 34, while other electrodes and sensors 36 are connected to the subject 38 to provide an EOG and an EMG signal.
  • the EEG machine or polysomnograph 34 passes analog signals from the electrodes and other sensors 36 through amplifiers and filters 39 and then transmits the amplified and filtered signals to the digital computer 32.
  • A/D converter 40 that receives, from the EEG machine or polysomnograph 34, the analog signals representing the signals present at the electrodes 36 attached to the subject 38.
  • the A/D converter 40 included in the digital computer 32 may be selected from various different types offered by several manufacturers such as the Burr-Brown model PCI-20098CI 12 bit A/D together with a Burr-Brown model PCI-20002M- 1 analog expander.
  • the A/D converter 40 included in the digital computer 32 converts the analog EEG, EOG and EMG signals into binary numbers every 5 to 10 milliseconds, and then stores the digitized value into a memory 41 of the digital computer 32. While these analog signals are preferably converted into digital values every 5 to 10 milliseconds, because the EEG and EOG signals have significant information up to 200 Hz, it may be beneficial to convert a sample of these signals into digital form as frequently as every 2.5 milliseconds. Alternatively, the EMG signal may have significant information up to 600 Hz which might require converting its signal every 0.8 milliseconds.
  • the A/D converter 40 of the preferred embodiment is capable of simultaneously receiving and digitizing up to 32 different signals, other signals frequently used in the scoring of sleep such as EKG and respiratory measures such as airflow, thoracic and abdominal effort, and blood oxygen saturation, Sa02, may also be concurrently digitized and stored into the memory 41 of the digital computer 32.
  • the signals are being digitized by the A/D converter 40 under the control of a sleep analysis computer program executed by the digital computer 32, they may be displayed on a high resolution color video monitor 42 connected to the digital computer 32. Also, as the signals are being digitized they are stored onto computer disk drives 44. While the computer disk drives 44 preferably include a Write Once-Read Many ("WORM") large capacity optical disk, other types of disk memories such as floppy-disks, removable cartridge disks and/or fixed, internal hard-disks may also be included in the computer system 30.
  • the digital computer system 30 also includes a keyboard 52 and a mouse 54 that an operator uses in interacting with and controlling the operation of the digital computer 32 for recording and analyzing sleep. In addition to the video monitor 42 for displaying the recorded data and the results of its analysis, the digital computer system 30 may also include a printer 56 and/or a chart recorder 58 for producing permanent, human readable copies of displays appearing on the video monitor 42.
  • the sleep analysis computer program executed by the digital computer 32 that controls the overall operation of the computer system 30 is invoked by a command to an operating system, MS-DOS, running on the digital computer 32.
  • This sleep analysis computer program is organized as a series of menus presented to the operator on the video monitor 42.
  • the operator selects an item from the menu presently displayed on the video monitor 42.
  • each menu option name includes an uppercase, or capitalized, letter. The option may be selected directly by pressing the corresponding key on the keyboard 52.
  • the sleep analysis computer program responds to each successive menu selection by performing the selected action which may be either the execution of a program function, providing the display of another menu from which additional selections may be made, or providing access to a set of commands.
  • FIG. 2 depicts the hierarchy of menus provided by the sleep analysis computer program illustrating how menus are invoked from other menus.
  • a main menu 62 which provides the only access into and out of the program.
  • a data collection menu 64 and a data analysis menu 66, which are the primary menus for controlling the program's operation.
  • a temporary exit menu 68 that allows temporarily suspending execution of the sleep analysis computer program and returning control of the digital computer 32 back to the operating system MS-DOS.
  • Execution of the sleep analysis computer program may be resumed precisely at the point of exit if it has been exited to MS-DOS through the temporary exit menu 68. Conversely, execution of the sleep analysis program may not be so resumed if an exit menu 72 is selected from the main menu 62.
  • Selecting collection in the main menu 62 puts the sleep analysis computer program in the data collection mode and causes the collection menu 64 to be displayed.
  • the second way of preparing the computer program for data collection is to re-use a previously stored system protocol. Except as expressly noted below, the following discussion of how an operator sets the data collection parameters is the same both for data collection and for preparing a system protocol that is to be saved for re-use.
  • an operator selects a file menu 74 from the collection menu 64.
  • the operator selects a subject information menu 76.
  • the operator enters information about the subject 38 into fields provided in the subject information menu 38 together with an MS-DOS name for the file in which the collected data will be stored and the length of time for which data is to be collected.
  • the operator enters the number of data channels for which physiological signals are to be saved to the computer disk drives 44 at the subject information menu 76. Having entered this information and/or parameters at the subject information menu 76, the operator then returns to the file menu 74 by pressing either the "ESC" key on the keyboard 52 or the right hand button on the mouse 54. If a previously stored data collection protocol is to be re-used, at the file menu 74 the operator selects a load menu 78, loads a previously stored system protocol, and returns to the file menu 74. The operator then returns to the collection menu 64 by pressing either the "ESC" key on the keyboard 52 or the right hand button on the mouse 54.
  • an operator Having returned to the collection menu 64, an operator then selects an amps menu 80 to display, on a channel-by-channel basis, the current values assigned to parameters for the amplifiers in the EEG machine or polysomnograph 34.
  • the amplifiers in the EEG machine or polysomnograph 34 are set to a gain of 20,000.
  • the operator uses keyboard 54 and/or the mouse 54 in assigning the proper values to these parameters. After the amplifier parameters for all the channels have been specified, the operator then returns to the collection menu 64.
  • the collection montage menu 84 permits the operator to specify an association between a particular channel of binary data coming from the A/D converter 39 and a channel of data displayed on the video monitor 42 and recorded in a file on the disk drives 44.
  • the collection montage menu 84 actually permits the operator to specify an association between a particular physiological signal originating at the subject 38 and a channel of data displayed on the video monitor 42 and recorded in a file on the disk drives 44.
  • the collection montage menu 84 also permits an operator to specify that a particular data channel will display and record algebraic combinations of specified physiological signals from the subject 38, and/or that a particular data channel will display and record an average of signals from several electrodes 36 attached to the subject 38.
  • an operator may then select a display format menu 86. If the operator does not specify a different display format using the display format menu 86, while the data is being collected the computer program displays the data on the video monitor 42 in a polygraph format such as that depicted in FIG. 3.
  • the polygraph format data is displayed on a rectangular waveform display grid 88 in one thirty second swath across almost the entire width of the video monitor 42. Displayed on the video monitor 42 in a rectangular area 92 immediately to the left of the waveform display grid 88 are data channel labels while voltage scaling factors appear in a rectangular area 94 immediately to the right of the waveform display grid 88.
  • the data appearing in the waveform display grid 88 of the polygraph format appears much the same as it would appear in the traditional paper strip chart recording.
  • the operator may select other formats, to be described below, in which the data will be displayed during collection. After having specified the format in which data will be displayed during collection, the operator returns to the collection menu 64.
  • an operator After selecting the display format at the display format menu 86 and returning to the collection menu 64, an operator has completed specification of all the data collection parameters that would generally be provided by a system protocol. At this point the operator may save the protocol that has been specified by selecting, from the data collection menu 64, the file menu 74 followed by a save menu 96. At the save menu 96, the operator specifies that a system protocol is to be saved, assigns a MS-DOS file name for the new system protocol, and enters a label that describes the system protocol. After entering this data, the present data collection protocol is saved in an MD-DOS file on the computer disk drives 4.4 for subsequent re-use.
  • an operator now selects a calibration menu 98, and from that menu selects a calibration collection menu 102.
  • the calibration collection menu 102 allows the operator to calibrate the various channels of the EEG machine or polysomnograph 34 and of the digital computer 32 that will be used in recording the physiological signals.
  • the operator successively supplies an analog electrical signal having a known amplitude to each input of the EEG machine or polysomnograph 34 while simultaneously entering data pertinent to the calibration procedure into the computer program. In this way the operator establishes a correlation between the amplitude of the physiological signals at the subject 38 and those displayed on the video monitor 42 and recorded in files on the disk drives 44.
  • the operator commences data collection by selecting a start option in the data collection menu 64. A short time after data collection begins, that data will begin appearing on the video monitor 42 in format selected by the operator at the display format menu 86.
  • an operator may still select various options from the data collection menu 64 while the computer system 30 records data from the subject 38. For example, the operator may choose a -scale menu 112 from the data collection menu 64 which allows changing the vertical scale at which the various signals appear in the waveform display grid 88. If an operator wants to change the format in which the data is displayed during data collection, that may be accomplished by selecting the display format menu 86 from data collection menu 64.
  • an operator wants to review previously recorded data while simultaneously continuing to record data, he may do so by selecting a time menu 114 from the collection menu 64 and specifying the time for which recorded data is to be replayed. The operator may also specify whether the replayed data is to occupy the entire data display area of the video monitor 42, or whether the replayed data is to appear in only a portion of that display area while the data being recorded continues to be displayed in the remainder of that area. The operator may choose to view the replayed data in any of the various display formats described herein below in connection with data analysis. Accordingly, during data collection an operator has full access to all of the various data analysis features provided by the computer program.
  • an operator may select an option on the data collection menu 64 that pauses data collection.
  • the waveform display continues as does data storage on the computer disk drives 44 but the physiological signals are set to zero volts.
  • the operator may resume further data collection at any time by pressing the ESC key on the keyboard 52 or the right button on the mouse 54.
  • the operator may also select an option on the data collection menu 64 that halts data collection entirely. Halting data collection may also be accomplished by pressing either the ESC key on the keyboard 52 or the right button on the mouse 54.
  • an operator may select a comment menu 116 from the data collection menu 64.
  • the comment menu 116 allows the operator to enter a text message, and to correlate that comment with the thirty second time interval of a single epoch. As described in greater detail below, these comments may be used subsequently to locate and display data recorded for the epoch with which the comment is associated. Accordingly, associating comments with particular epochs in the recorded data effectively allows subsequent random access to the data during replay.
  • the operator may select an option on the data collection menu 64 that causes the computer program to ignore input signals from both the mouse 54 and keyboard 52 except for one particular unique and obscure key combination on the keyboard 52. From the operator's perspective, this selection from the data collection menu 64 makes it appear as though the keyboard 52 and the mouse 54 have been locked. If during data collection the operator refrains from entering the particular unique and obscure key combination on the keyboard 52 that unlocks both it and the mouse 54, they are automatically unlocked at the end of the previously specified data collection interval.
  • An operator of the sleep analysis digital computer system 30 may analyze previously collected data in five different ways. Thus, by selecting the appropriate options from various menus an operator may display the raw data as it was collected, analyze raw data for sleep stage scoring and to identify respiratory disturbances, display and interpret the results of sleep scoring, save the scoring results to the disk drives 44, and retrieve prior scoring results from the disk drives 44.
  • an operator To display the raw data as it was collected, an operator first selects the data analysis menu 66 from the main menu 62 which causes the polygraph format display, illustrated in FIG. 3, to appear on the video monitor 42. As depicted in FIG. 3, appearing in a horizontal menu selection bar 118 across the top of the video monitor 42 are the various menu selections that are allowed from the data analysis menu 66. In displaying the raw data, from the data analysis menu 66 the operator then selects the file menu 74 followed by the load menu 78 as illustrated in FIG. 2. At the load menu 78, an operator specifies the particular file of previously collected data to be loaded. Having thus loaded the raw data, similar to data collection there are two ways an operator may prepare the computer program for data analysis. The first way is to interactively set up a display protocol by reviewing each program option affecting the display of sleep data, adjusting parameter values if necessary. The second way of preparing the computer program to analyze previously collected data is to re-use a previously stored display protocol.
  • an operator In interactively preparing the computer program for data analysis or preparing a display protocol, if the display format presently appearing on the video monitor 42 is not that desired, an operator first selects the display format menu 86 from the data analysis menu 66. At the display format menu 86, the operator may choose among several different display formats that one in which the data will be displayed.
  • the operator may specify a number of signal channels up to a maximum of thirty-two to appear on the video monitor 42. Furthermore, the operator may select among three different modes in which new data will replace that presently being displayed: normal polygraph mode, scroll polygraph mode and page polygraph mode.
  • normal polygraph mode new data overwrites the earlier data from left to right across the waveform display grid 88.
  • scroll polygraph mode new data appears along the right edge of the waveform display grid 88 while the earlier data moves progressively away from the right edge toward the left edge thereby effectively pushing the oldest data off the left edge of the waveform display grid 88.
  • the visual appearance of the scroll polygraph mode of display is similar to the operation of the traditional multi-channel ink- on-paper recording.
  • page polygraph mode the data displayed in the entire waveform display grid 88 is entirely overwritten all at one time.
  • the time base for the display in seconds per major division across the width of the video monitor 42 appears in a rectangular box 122 near the lower right corner of FIG. 3.
  • Also displayed in a rectangular box 124 at the lower right corner of the video monitor 42 is the number of the epoch which is currently being displayed.
  • a time display 126 of the time for the epoch presently appearing on the video monitor 42.
  • paging icons 132, 134, 136 and 138 Appearing at the bottom of the screen immediately below the waveform display grid 88 are paging icons 132, 134, 136 and 138.
  • the left pointing icons 132 and 136, or their keyboard equivalents move the data displayed on the video monitor 42 toward the beginning of the raw data
  • right pointing icons 134 and 138, or their keyboard equivalents move the displayed data toward the end of the raw data.
  • the single arrowed icons 136 and 138, or their keyboard equivalents move one epoch for each successive selection while the double arrowed icons 132 and 134 ' cause continuous and uninterrupted paging through successive epochs in the raw data file.
  • the keyboard equivalent of the icon 132 is the shifted left pointing arrow.
  • the keyboard equivalent to the icon 134 is the shifted right pointing arrow.
  • the un- shifted left pointing arrow on the keyboard is equivalent to the icon 136 while the un-shifted right pointing arrow on the keyboard is equivalent to the icon 138.
  • Another display format that may be selected from the display format menu 86 is a staging display format illustrated in FIG. 4.
  • the staging format a single thirty second epoch of the three channels of the physiological signals that are the basis for sleep stage scoring, i.e. EEG, EOG and EMG, are displayed on the video monitor 42.
  • This single thirty second epoch of data is displayed in three successive horizontal segments or swaths 142 of waveform display grids, one below the other, across the width of the video monitor 42.
  • each swath 142 Appearing in a rectangular box 144 at the left end of each swath 142 are labels identifying the EEG, EOG and EMG signals. Analogous to the rectangular area 94 in the polygraph display format, appearing in a rectangular box 146 at the right end of each swath 142 are the voltage scaling factors for each of the physiological signals. Each of the swaths 142 displays one-third of the thirty second epoch, i.e. ten seconds. Accordingly, each major division across the width of the video monitor 42 displays a one second interval of the physiological signals as appears in the rectangular box 122.
  • FIG. 5 illustrates a display format used in respiratory analysis that may be selected from the display format menu 86. Similar to the staging display format illustrated in FIG. 4, the respiratory display format of FIG. 5 presents three successive horizontal segments or swaths 142 of waveform display grids, one below the other, across the width of the video monitor 42. Displayed in each of the swaths 142 are four physiological signals identified in rectangular boxes 152 located at the left end of each of the swaths 142, i.e. air flow, thorax and abdomen respiratory effort channels, and blood-oxygen saturation. As with both the polygraph and staging display formats, voltage scaling factors for each of the signals appear in rectangular boxes 146 at the right end of each swath 142.
  • each swath 142 displays two minutes of the four physiological signals thereby presenting a total of six minutes of data on the video monitor 42. Accordingly, a time base of ten seconds per major division appears in the rectangular box 122. Appearing above the left end of each swath 142 is a number 154 for the first thirty second epoch in each swath 142. Above the right end of each swath 142 appears a number 156 that indicates the time of the data appearing at the right end of each swath 142.
  • event markers in the respiratory display format indicate the presence of respiratory disturbances.
  • Events are marked with an alphabetic letter 158 from which a bar 162 extends horizontally to the right.
  • the color of both the letter and the bar displayed on the color video monitor 42 indicates the nature of the respiratory disturbance: red for apnea or magenta for hypopnea.
  • the alphabetic letter indicates the type of the apnea or hypopnea: "C" for central, "O” for obstructive, and "M” for mixed.
  • the length of the line extending from the alphabetic letter corresponds to the length of the respiratory disturbance.
  • FIG. 6 illustrates a rectangularly shaped respiratory disturbance log 168 that may be selected from the display format menu 86.
  • the respiratory disturbance log 168 is superimposed over a portion of other displays such as the respiratory display format illustrated in FIG. 5.
  • the following table summarizes the data presented in the eleven vertical columns across the width of the respiratory disturbance log 168.
  • Afct The presence or absence of an artifact A/H The nature of respiratory disturbance: "AP” for apnea and "HY" for hypopnea
  • Selecting the respiratory disturbance log display format also activates several function keys on the keyboard 52. Repetitively pressing function key 3 allow moving the respiratory disturbance log 168 to either the top, middle or bottom of the video monitor. By moving the respiratory disturbance log 168 vertically on the video monitor 42, an. operator may view any part of the data displayed in the background display format without removing the respiratory disturbance log 168. Highlighting a particular event listed in the respiratory disturbance log 168 using the mouse 54 and then pressing function key 10 causes the background display format to present the physiological signals at the time of the highlighted event.
  • FIG. 7 illustrates another display format, analogous to the display format of FIG. 4, that also has three horizontal segments or swaths 142 of waveform display grids, one below the other, across the width of the video monitor 42.
  • FIG. 7 displays the raw data for three epochs at different times as indicated by numbers 172 located above the right end of each of the swaths 142.
  • the number 154 for each of the epochs appearing on the video monitor 42 appears above the left end of each of the swaths 142.
  • an operator may compare physiological signals for arbitrarily selected epochs.
  • the operator selects the montage menu 82 followed by a display montage menu 176 as depicted in FIG. 2.
  • the operator specifies the various channels of physiological signals.that are to be displayed, the order of the 35
  • physiological signals from top to bottom on the display format, together with the label appearing to the left of each waveform that identifies it.
  • care must be exercised to insure that the proper channel of physiological data is specified so automatic sleep scoring and respiratory analysis will operate properly.
  • the proper assignment of the physiological signals is described below in connection with automatic sleep scoring.
  • the operator After selecting the display format at the display format menu 86 and specifying the various physiological signals at the montage menu 82, the operator has completed specifying all the data analysis parameters that would generally be provided by a display protocol.
  • an operator may save the display protocol that has been developed by selecting, from the data analysis menu J 66, the file menu 74 followed by the save menu 96.
  • the operator specifies that a display protocol is to be saved, assigns a MS-DOS file name for the new display protocol, and enters a label that describes the display protocol. After entering this information, the present display protocol is saved in an MD- DOS file on the computer disk drives 44 for subsequent re-use.
  • the computer system 30 is now ready to display previously collected data for analysis.
  • An. operator causes data to be displayed on the video monitor 42 by moving through the previously collected raw data that is now stored on the disk drives 44. There are several alternative ways an operator may specify the time of the recorded raw data to be displayed.
  • One way of displaying the recorded data is to select the time menu 114 from the data analysis menu 66. At the time menu 114 the operator enters the number of the desired epoch and shortly thereafter the physiological signals for that epoch are displayed on the video monitor 42 in the previously selected display format.
  • an operator can use the paging icons 132 and 134, or their keyboard equivalents, to page continuously either backward or forward through the recorded data.
  • An operator may stop contin ⁇ uous paging either by pressing the ESC key on the keyboard 52 or the right button on the mouse 54.
  • an operator can page backward or forward through the data one epoch at a time using the paging icons 136 or 138 or their keyboard equivalents.
  • comments have been associated with the recorded data
  • an operator can use them to move directly to the data with which the comment is associated.
  • the operator selects the comment menu 116 from the data analysis menu 66.
  • the operator selects a position option and a box appears on the video monitor 42 listing each of the comments and their respective temporal location within the recorded data. The operator then selects the desired comment after which the recorded data for the epoch with which that comment is associated appears on the video monitor 42.
  • an operator selects the scale menu 112 from the data analysis menu 66. Having selected the scale menu 112, the operator then select the channels for the physiological signals whose scale is to be raised or lowered. Raising the scale increases the height of the selected physiological signal while lowering the scale decreases the waveform's height.
  • an operator may review any textual comments added to the data during data collection or during a prior data analysis session, or insert a textual comment to be associated with previously recorded data by selecting the comment menu 116 from the data analysis menu 66.
  • Such comments are displayed in the lower right corner of the video monitor 42 when the data is displayed for the epoch with which the comment has been applied.
  • an operator may also delete comments.
  • deleting a comment a box analogous to the respiratory disturbance log 168 listing each comment and its temporal location within the data file appears on the video monitor 42 over the data display. The operator then uses the mouse 54 to highlight the comment to be deleted. Scoring
  • such data can be automatically scored for sleep staging and for respiratory analysis by selecting a scoring menu 192 from the data analysis menu 66.
  • sleep stages can be scored manually using a manual scoring mode, and previously scored sleep stages can be overwritten using a revise scoring mode.
  • raw physiological data may be scored, it must first be loaded and displayed on the video monitor 42 for data display as described above.
  • the automatic sleep staging and respiratory analysis require a pre-established assignment of particular physiological signals, e.g.
  • the EEG channel of physiological data must be assigned to the first position highest in the swaths 142 of the staging display format illustrated in FIG. 4.
  • the EOG channel must be assigned to the second position in the middle of the swaths 142 while the EMG channel must be assigned to the third position at the bottom of the swaths 142 of the staging display format.
  • the air flow channel of physiological data must be assigned to the first position highest in the swaths 142 of the respiratory display format illustrated in FIG. 5.
  • the second and third positions about the middle of the swaths 142 must be assigned to channels of physiological data indicative of respiratory effort. Typically the second position indicates thorax effort while the third position indicates abdominal effort.
  • the oxygen saturation (Sa02) must be assigned to the fourth position lowest on the swaths 142 of the respiratory display format.
  • FIG. 8 illustrates a matrix display for the automatic sleep scoring parameters that an operator uses in assigning values to those parameters.
  • the display of FIG. 8 allows an operator to specify horizontal rows of parameters used in automatically identifying each of the following sleep scoring waveform events; alpha, spindle, slow wave, K complex REM and high EMG.
  • the matrix display of FIG. 8 includes an alpha row 202, a spindle row 204, a slow wave row 206, a K complex row 208, REM row 212, and a high EMG row 214.
  • alpha, spindle, slow wave, K complex REM and high EMG are characterized at least in part by a threshold voltage amplitude parameter appearing in a vertical column 222 of the matrix display of FIG. 8.
  • a threshold voltage amplitude parameter appearing in a vertical column 222 of the matrix display of FIG. 8.
  • the alpha row 202, spindle row 204, slow wave row 206, K complex row 208 and REM row 212 events are also characterized by a lower frequency parameter and an upper frequency parameter appearing respectively in vertical columns 224 and 226 of the matrix display of FIG. 8.
  • the alpha row 202 and spindle row 204 events are also characterized by a regularity parameter also appearing in a vertical column 228 of the matrix display of FIG. 8.
  • a value must be specified for each of the parameters at the respective intersections of the horizontal rows 202, 204, 206, 208, 212 and 214 with the vertical columns 222, 224, 226 and 228 in which parameters appear in FIG. 8. Revised values for these parameters may be entered by choosing the appropriate entry appearing in a parameter editing field 232 displayed at the right of FIG. 8 which duplicates the parameter display in the intersections of rows 202 through 214 with columns 222 through 228. Each parameter to be changed is selected using the mouse 54 or the keyboard 52 and then.a new numeric value is entered using the keyboard 52.
  • the editing field 232 may also be used to display other sets of automatic analysis parameters read from the disk drives 44.
  • the operator After an operator has specified the values for the automatic analysis parameters in the editing field 232 either by reading a set of previously saved parameters, by entering them directly, or by a combination thereof, the operator then requests that the parameter values in the editing field 232 be transferred to the intersections of the horizontal rows 202, 204, 206, 208, 212 and 214 with the vertical columns 222, 224, 226 and 228.
  • the operator By transferring the parameters from the editing field 232 to the intersections of the rows and columns the operator makes them the values that will be used in automatically scoring the raw data.
  • sets of scoring parameters may also be saved on the disk drives 44 for re ⁇ use at some subsequent time when they are then re-loaded.
  • the parameters respectively specified in the rows 202 through 208 are used independently of each other in automatically identifying such events. Conversely, the parameters in the rows 212 and 214 are used together in automatically identifying REM events.
  • the occurrence of events characterized by a high frequency EEG signal i.e. alpha and spindle, are identified by analyzing peak values in the raw EEG data.
  • each one-half second interval of the raw EEG signal is processed to determine the time intervals between successive peak values in the raw EEG data. If the interval between the peak values is much too short, then such an interval is eliminated from further analysis as being due to some artifact.
  • the intervals determined by this process are then further analyzed to determine the mean frequency throughout the one-half second interval and also the highest and lowest momentary frequency during that interval.
  • the difference between the highest and lowest momentary frequency throughout the one-half second interval is compared with the regularity parameter.
  • a value of zero for the regularity parameter assures the acceptance of each event which satisfies the amplitude threshold and frequency limits.
  • a value of five for the regularity parameter assures the rejection of all events which satisfy the amplitude threshold and frequency limits. Increasingly higher values of the regularity parameter between its limits of zero and five cause the rejection of events having progressively smaller differences between the highest and lowest momentary frequency.
  • events characterized by a low frequency EEG signal i.e. slow wave and K complex EEG events and REM events
  • the data are first filtered and smoothed to eliminate high frequency components. After filtering and smoothing, the zero crossings of the respective signals are analyzed to identify events satisfying both the specified amplitude threshold and frequency limits. While the slow wave and K complex EEG events are identi ⁇ fied solely by satisfying the criteria specified by the parameters in rows 206 and 208 of FIG.
  • REM events are identified only if the criteria specified by the parameters in row 212 are satisfied during intervals in which there is a low EMG signal. Consequently, even though the raw REM data has a sufficiently high amplitude and has a frequency lying within the specified frequency range, the computer program will not score that data as a REM event unless the EMG data is lower than the threshold value.
  • Automatic respiratory analysis identifies events of respiratory dysfunction in the raw respiratory data and assigns those events to the respiratory disturbance log illustrated in FIG. 6.
  • the computer program compares the present airflow with a "moving window" baseline mean amplitude for airflow. If the present airflow drops 20% below the baseline value while remaining above 50% of the baseline value and remains within the range of 20% to 50% below the baseline value for 10 seconds, then an apnea event has begun. Alternatively, if the present airflow drops 50% below the baseline value and remains below that level for 10 seconds. then a hypopnea event has begun. An apnea event or a hypopnea event ends when the present airflow returns to the baseline value existing prior to the event's commencement.
  • Events of apnea or hypopnea are classified as central, obstructive or mixed based on data in either of the respiratory effort data channels, i.e. the thorax or the abdominal data. If the muscles of either the thorax or the abdomen are inactive throughout the event, then it is classified as central. If the muscles are active throughout the event, then it is classified as obstructive. If the muscles are partially active during the event, then it is classified as mixed.
  • an operator selects the scoring menu 192 from the data analysis menu 66 and then specifies either an automatic stage scoring mode or an automatic respiratory mode, or both.
  • the present status of these modes is respectively indicated in rectangular boxes 242 and 244 located in the upper right hand corners of various display formats such as the polygraph display format illustrated in FIG. 3, the staging display format illustrated in FIG. 4, and the respiratory display format illustrated in FIG. 5.
  • the word "AUTO” appears in the box 242.
  • the word "AUTO” appears in the box 244.
  • each epoch appearing on the video monitor 42 causes each epoch appearing on the video monitor 42 to be scored.
  • characters and numbers displayed in a horizontal stage scoring bar 248 across the top of the screen immediately beneath the menu selection bar 118 and immediately above the waveform display grid 88 or the uppermost swaths 142 indicates the sleep stage score for the epoch.
  • the following table lists the characters and numbers that may appear in the stage scoring bar 248 together with the corresponding sleep stage.
  • an operator may "teach" the data analysis portion of the computer program how to score the raw data. This process is repeated one after the other to "teach” the data analysis portion of the computer program suitable analysis parameters for each of the various different types of events, i.e. alpha, spindle, slow wave, K complex, REM and high EMG.
  • the operator initially specifies comparatively relaxed parameters, i.e. a low amplitude in column 222, a wide frequency range in columns 224 and 226, and a regularity of zero in column 228.
  • the data analysis program then scores one epoch for alpha events, usually the first epoch in the raw data because that epoch will usually contain alpha events. After scoring an epoch for alpha, the data analysis program then displays the results and allows the operator to successively specify whether each event has been identified correctly or incorrectly. After all the events in an epoch have been classified as being correctly or incorrectly identified, the operator can decide to score another epoch or terminate learning for this particular type of event. By this process, the data analysis portion of the computer program collects a set of prototypical events whose scoring is acceptable to the operator and a set of events which the operator has rejected. Using an operator's classification of events, the computer program then adjusts the automatic analysis parameters to conform with that classification.
  • This adjustment of the automatic analysis parameters is possible because the operator's acceptance and rejection of events effectively compiles amplitude and mean frequency data both for the accepted and for the rejected events.
  • the computer program then uses this data to assign values for those parameters that are compatible with the operator's classification of the events. Two different methods may be employed to assign these values to the parameters using the data collected by the computer program, a simpler one and a slightly more complicated one.
  • the simpler method for assigning values to the parameters used for event identification employs only the data for the accepted events.
  • the minimum amplitude for the accepted events, the minimum mean frequency for those events and the maximum mean frequency for those events are assigned as the values for the respective parameters in columns 222, 224 and 226.
  • the more complicated method for assigning values to the parameters used for event identification uses both the data for the accepted events and for the rejected events. This more complicated method determines the range of overlapping values for each parameter between the accepted and the rejected events. The value of that parameter is then set equal to the value at the center of the overlapping range. Thus, for the amplitude parameter, the value assigned to column 222 is one-half of the minimum value of the accepted events plus the maximum value of the rejected events. For the assignment of the lower and upper frequency limits respectively in columns 224 and 226, the rejected events are divided into those having a mean frequency lower than the average of the accepted events and those having a mean frequency higher than the average of the accepted events.
  • the value then assigned to the lower frequency limit in column 224 is one-half of the minimum value of the mean frequency for the accepted events plus the maximum value of the mean frequency for the rejected events having a mean frequency lower than the average for the accepted events.
  • the value then assigned to the upper frequency limit in column 226 is one-half of the maximum value of the mean frequency for the accepted events plus the minimum value of the mean frequency for the rejected events having a mean frequency higher than the average for the accepted events.
  • data from the operator's event classification are used to assign values for the amplitude and the lower and upper frequency parameters that distinguish between those events accepted by an operator and those rejected by the operator.
  • the parameters that the computer program has "learned" in this way are then used to score the raw data in substantially the same way as the operator would score it.
  • an operator may interactive- ly “teach" the computer the particular way in which a subject's sleep is to be scored.
  • the entire file of raw physiological data may be automatically scored if so specified at the scoring menu 192.
  • automatic scoring may be restricted to continuous segments that are only a fraction of the raw data.
  • the scoring menu 192 also permits selecting manual sleep stage scoring. If manual sleep stage scoring is selected, the word "MANUAL" appears in the box 242 together with an array of icons consisting of boxed letters and numbers, not illustrated in FIGs. 3, 4 or 5, that are located along the right hand edge of the video monitor 42. An operator can select the appropriate one of these icons with the mouse 54 to manually score an epoch. Alternatively, an operator may score the epoch by pressing the key on the keyboard that corresponds to the letter or number displayed in the icon. After a score has been specified for an epoch, all successive epochs displayed on the video monitor 42 are assigned that same score until the operator selects a different score for the epoch then being displayed.
  • the score previously assigned to epochs may be changed in the same manner as that described above for manual scoring. As with sleep staging, respiratory disturbances may also be scored manually and any prior scoring may be revised.
  • the display format menu 86 provides other display formats that are specially adapted to display the results of sleep scoring and respiratory analysis.
  • the first of these display formats is the hypnogram display format illustrated in FIG. 9.
  • the hypnogram display format presents sleep stage scoring as a function of time. Sleep stages are indicated along a vertical axis 262 by the same characters and numbers as those described above in connection with the stage scoring bar 248 except for the "U," undefined, score. Elapsed time (in hours) is indicated along a horizontal time axis 264. A plurality of vertical line segments 266 extending upward from the time axis 264 indicate the stage of sleep occurring during each epoch.
  • hypnogram display format In the hypnogram display format four cursor icons 272, 274, 276 and 278, located near the bottom of the display on the video monitor 42, or their keyboard equivalents, move a vertical cursor 282 back and forth along the horizontal time axis 264 in the same manner as the paging icons 132 through 138. Displayed in the hypnogram display format immediately to the right of the horizontal time axis 264 and slightly above the time display 126 for the current cursor position appears a sleep stage score 286 for the present cursor position.
  • FIG. 10 Another display format that is specially adapted for displaying the results of scoring which may be selected from the display format menu 86 is the summary display format illustrated in FIG. 10.
  • the particular summary display format illustrated in FIG. 10 presents in three separate rectangular areas extending across the width of the video monitor 42 and positioned vertically along its height a combination of data taken from the hypnogram display format, from the respiratory disturbance log - display format, and the respiratory display format.
  • the summary display format includes a unique menu presented in the menu selection bar 118.
  • the "Window Setup" command in the summary display format menu allows an operator to adjust the type of plot that appears in each of the three areas, the time base along horizontal time axes 264a, 264b and 264c respectively displayed near the bottom of each area. and the colors used in the hypnogram plot.
  • the "Window Setup” command also allows unlocking vertical cursors 282a, 282b and 282c so that they either move independently within each of the three areas or locking them so they move in unison across all three areas.
  • the "Set File Position" command in the summary display format allows an operator to set the active epoch to the present cursor position.
  • the raw data for that epoch will be displayed automatically if one of the display formats such as the polygraph, staging or respiratory display formats are then selected to replace the summary display format.
  • the "Change Active Window” command in the summary display format allows selecting which of the cursors 282a, 282b or 282c in three areas will control the "Set File Position” command. This command also allows specifying which of the cursors 282a, 282b or 282c will move in response to commands from cursor icons 272 through 278, or their keyboard equivalents.
  • An arrow 292 located to the left of one of the horizontal axes 264a, 264b or 264c indicates which area is presently active.
  • Displays located immediately to the right of the of each of the axes 264a, 264b and 264c respectively present information pertinent to the plot displayed along the corresponding axis 264a, 264b or 264c. Accordingly, displayed to the right of the axis 264a along which a hypnogram is plotted are a time display 126a for the position of the cursor 282a along the axis 264a and the sleep stage score 286 for that position of the cursor 282a.
  • a respiratory disturbance plot appears immediately below the hypnogram in the particular summary display format illustrated in FIG. 10.
  • This respiratory disturbance plot displays apneas, hypopneas and arousals along the horizontal time axis 264b.
  • a plurality of vertical line segments 296 are displayed to the right along the axis 264b from the words "Apnea" and "Hypopnea,” that are located immediately to the left of a vertical axis 298.
  • Each vertical line segment indicates the occurrence of a respiratory disturbance at the corresponding time and the type of disturbance that occurred.
  • each of these vertical line segments indicates the time within the epoch at which the disturbance occurred.
  • the color of the line segment indicates whether the respirator disturbance was central (red), obstructive (blue) or mixed (green).
  • the length of the vertical line segments represent the duration of the respiratory disturbance.
  • a respiratory disturbance is accompanied by arousal, that will be indicated by the presence of a vertical line segment at the appropriate location along the axis 264 to the right of the word "Arousal.”
  • a time display 126b on the respiratory disturbance plot immediately to the right of the axis 264b displays the time for the position of the cursor 282b along the axis 264b.
  • three encodings 302 indicating the type of disturbances(s) that occurred during the epoch at which the cursor 282b is presently located.
  • Each encoding 302 is made up of three alphabetic characters separated by "/" punctuations.
  • the vertical position of the encodings indicates their respective order of occurrence within the epoch with the earliest respiratory disturbance encoded at the top and the latest one encoded at the bottom.
  • the first character in each encoding indicates whether the disturbance was a apnea (A) or a hypopnea (H) .
  • the second character in each encoding indicates whether the disturbance was central (C), obstructive (O) or mixed (M) .
  • the third character in each encoding indicates whether the disturbance was accompanied by arousal (Y) or was not accompanied by arousal (N).
  • a blood oxygen saturation plot appears immediately below the respiratory disturbance plot in the particular summary display format illustrated in FIG. 10.
  • Extending horizontally to the right of a vertical axis 306 that represents blood oxygen saturation, i.e. Sa02, increasing from 0% to 100%. appear a plurality of vertical line segments 308.
  • Each vertical line segment presents the minimum and maximum oxygen saturation within an epoch.
  • the vertical line segment's position along the axis 264c correlates the epoch's time.
  • a time display 126c on the oxygen saturation plot immediately to the left of the axis 264c displays the time for the position of the cursor 282c along the axis 264b.
  • a minimum blood oxygen saturation 312 for the epoch at which the cursor 282c is positioned appears immediately above the minimum blood oxygen saturation 312 for that same epoch.
  • FIG. 11 illustrates another display format, which may be se ⁇ lected from the display format menu 86, that displays several different physiological signals occurring at different times in the raw data.
  • two different swaths 142 of respiratory analysis raw data signals are displayed for two relatively short time intervals that are widely separated in time.
  • a blood oxygen saturation plot similar to that described previously in connection with FIG. 10.
  • a pair of vertical cursors 322a and 322b on the blood oxygen saturation plot identify the time interval for which the respiratory analysis raw data signals are displayed in the uppermost swath 142.
  • FIG. 12 as well as FIG.
  • FIG. 11 illustrate display formats in which two different physiological signals are displayed over differing durations.
  • two horizontal swaths 142 of the EEG, EOG and EMG physiological signals are displayed in the same scale as that illustrated in the display format illustrated in FIG. 4.
  • FIG. 11 in this particular illustration of this display format beneath the two swaths 142 appears a blood oxygen saturation plot.
  • FIGs. 10 through 12 are particularly useful in correlating respiratory disturbances with the various physiological signals such as Sa02, sleep staging, arousal and the EEG and EMG signals.
  • the computer program will cumulate the time for each different type of event through out a night's sleep.
  • the computer program will also count the number of times each different type of event occurs through a night's sleep.
  • a graphic display of either or both of these cumulative data can be selected from the display format menu
  • the computer program may also automatically select the parameters used for event identification described above in connection with FIG. 8.
  • an operator may enter certain physical characteristics for the subject 38 such as age, medication, prior sleep dysfunctions, diagnostic categories both physiological and psychological, and stress level.
  • the computer program will then use these characteristics to select an initial, trial data analysis protocol from a library of such protocols.
  • the parameters selected in this manner are then used in a trial scoring of a portion of the raw data either in the "learning" mode described above or directly using automatic scoring. If this trial is performed using automatic scoring, then the computer program may compare the overall results of that scoring with pre-established criteria to determine if those results are reasonable. For example, scoring must begin and end in the awake state. If the initial trial scoring parameters fail to produce this result different trial parameters must be selected.
  • stage 4 sleep if the trial scoring results in a hypnogram that reaches stages 1 and 2 of sleep but never gets to stage 4 sleep, this indicates that the trial parameters for identifying slow wave events need to be altered so the scoring results in stage 4 sleep. Similarly, if the scoring shows an excessive amount of stage 4 sleep, then the slow wave and alpha parameters must also be altered to decrease the amount of stage 4 sleep. If the trial scoring results in an excessive amount of stage 2 sleep, then the parameters for spindle, K complex and alpha must be altered to decrease the amount of stage 2 sleep.
  • a channel of physiological data may be collected from a microphone present in the room the subject 38, or by any other sensor which responds the generation of percepti ⁇ ble, audible sound produced by the subject 38. Since the strength of the signal produced by such a sensor itself constitutes a perceptible sound signal associated with the generation of audible sound by the subject 38, the mere amplitude of such a signal reveal the occurrence of snoring. Consequently, either the waveform produced by the sensor itself or only the envelope of that waveform may be included among the collected data. Moreover, this perceptible sound signal may only be recorded during epochs in which it exceeds a pre-established threshold.
  • the waveform of the audible sound is to be recorded directly, then that signal should be sampled at a frequency of 15 KHz. Alternatively, if only the envelope of the audible sound signal is to be recorded, a sampling rate of approximately 200 Hz is adequate.
  • snoring which is hazardous to a subject 38 may precede or correlate with events of apnea or hypopnea, or to reduction of the Sa02 level.
  • Such correlations between snoring and other events may be easily established after the raw physiological data has been scored for the stages of sleep and for respiratory disturbances.
  • the correlation between snoring and other events may either be identified analytically or using graphical displays of the recorded physiological signals and/or of their scoring.
  • the apparatus and computer program disclosed herein is capable of recording far more channels of data than are usually required merely for sleep analysis, by employing a larger number of EEG sensors 36 secured to the head of the subject 38 and recording the data from such sensors, the sleep analysis techniques disclosed above may be effectively combined in a single computer program with brain electrical activity analysis and mapping. Techniques for such brain electrical activity analysis and mapping which are also compatible with the sleep staging and respiratory analysis disclosed herein are described in U.S. Patents No.s 4,649,482, 4,744,029 and 4,862,359 which are all assigned to the assignee of the present application. Accordingly, those patents are hereby incorporated by reference as though fully set forth here.

Abstract

Appareil informatisé d'assistance à un opérateur lors de l'analyse des signaux physiologiques survenant pendant le sommeil et de l'évaluation des stades du sommeil. Afin d'enseigner à l'ordinateur le procédé d'analyse des signaux physiologiques et d'évaluer les stades du sommeil, l'opérateur établit les valeurs initiales des paramètres qui distinguent les événements dans les données enregistrées. Ensuite, on identifie les événements d'une partie des données enregistrées à l'aide des paramètres initiaux et l'on en affiche les résultats pour que l'opérateur puisse les consulter et classifier séparément les événements qui ont été correctement identifiés et ceux qui ont été incorrectement identifiés. A l'aide de cette classification, l'ordinateur ajuste les paramètres conformément aux événements correctement identifiés. Au lieu de cela, l'opérateur peut introduire des informations concernant des caractéristiques sélectionnées du sujet, par exemple son âge, son sexe, etc. Ensuite, on utilise ces caractéristiques physiques pour extraire un protocole initial d'une bibliothèque de protocoles préalablement enregistrés, puis l'on évalue les données enregistrées pour les signaux physiologiques à l'aide de ce protocole initial avant d'extraire un deuxième protocole de ladite bibliothèque en fonction des résultats de l'évaluation à l'aide du protocole initial. Les divers formats d'affichage du programme informatique permettent à un opérateur de visualiser de plusieurs façons différentes l'analyse assistée par ordinateur du sommeil et d'associer des textes de commentaire à des époques des données.
PCT/US1990/007189 1989-12-13 1990-12-12 Analyse assistee par ordinateur du sommeil WO1991009372A1 (fr)

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4339154A1 (de) * 1993-11-16 1995-05-18 Hewlett Packard Gmbh Anästhesie-Protokollsystem und Verfahren zum Steuern desselben
EP0678809A2 (fr) * 1994-04-13 1995-10-25 Becton, Dickinson and Company Dispositif pour l'automatisation du traitement par lots d'analyses de données
EP0705070A1 (fr) * 1993-06-23 1996-04-10 Aequitron Medical, Inc. Evaluation iterative du sommeil
WO1997014354A2 (fr) * 1995-10-16 1997-04-24 MAP Medizintechnik für Arzt und Patient GmbH Procede et dispositif pour l'analyse quantitative de troubles du sommeil
WO1998006326A1 (fr) * 1996-08-15 1998-02-19 Nellcor Puritan Bennett Incorporated Systemes de controle de patients
GB2381586A (en) * 2001-11-01 2003-05-07 Oxford Biosignals Ltd Electro-Oculographic Sleep Monitoring
WO2004028365A2 (fr) * 2002-09-20 2004-04-08 MCC Gesellschaft für Diagnosesysteme in Medizin und Technik mbH & Co. KG Procede et dispositif permettant de determiner un profil de sommeil
US7170994B2 (en) 2003-10-15 2007-01-30 Motorola, Inc. Method and apparatus for selecting an alert mode based on user biometrics
WO2011084394A1 (fr) * 2009-12-16 2011-07-14 Brainscope Company, Inc. Méthode et dispositif pour l'évaluation neurologique d'intervention et le guidage du traitement
US8364254B2 (en) 2009-01-28 2013-01-29 Brainscope Company, Inc. Method and device for probabilistic objective assessment of brain function
US9538949B2 (en) 2010-09-28 2017-01-10 Masimo Corporation Depth of consciousness monitor including oximeter
US9775545B2 (en) 2010-09-28 2017-10-03 Masimo Corporation Magnetic electrical connector for patient monitors
EP2589335A3 (fr) * 2003-04-10 2017-10-04 Adidas AG Systèmes et procédés de détection d'événements respiratoires
US10154815B2 (en) 2014-10-07 2018-12-18 Masimo Corporation Modular physiological sensors
US10321840B2 (en) 2009-08-14 2019-06-18 Brainscope Company, Inc. Development of fully-automated classifier builders for neurodiagnostic applications

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6600126B2 (ja) * 2014-03-25 2019-10-30 フクダ電子株式会社 生体信号処理装置およびその制御方法
JP6681399B2 (ja) * 2014-12-11 2020-04-15 コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. 徐波検出基準を調整するシステム及び方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4336810A (en) * 1980-09-30 1982-06-29 Del Mar Avionics Method and apparatus for arrhythmia analysis of ECG recordings
US4649482A (en) * 1984-08-31 1987-03-10 Bio-Logic Systems Corp. Brain electrical activity topographical mapping
US4739772A (en) * 1983-02-01 1988-04-26 Hokanson D Eugene Brain wave monitoring mechanism and method
US4776345A (en) * 1987-09-04 1988-10-11 Cns, Inc. Interactive determination of sleep stages
WO1988010093A1 (fr) * 1987-06-26 1988-12-29 Nicolet Instrument Corporation Procede et systeme pour l'analyse d'enregistrements polygraphiques physiologiques a long terme

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59125660A (ja) * 1983-01-06 1984-07-20 Nec Corp モニタ集積型半導体発光素子
JPS645088A (en) * 1987-06-29 1989-01-10 Toshiba Corp Semiconductor laser device
JPH0716079B2 (ja) * 1987-07-10 1995-02-22 松下電器産業株式会社 半導体レ−ザ装置
JPH0831653B2 (ja) * 1987-07-21 1996-03-27 国際電信電話株式会社 半導体レ−ザ

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4336810A (en) * 1980-09-30 1982-06-29 Del Mar Avionics Method and apparatus for arrhythmia analysis of ECG recordings
US4739772A (en) * 1983-02-01 1988-04-26 Hokanson D Eugene Brain wave monitoring mechanism and method
US4649482A (en) * 1984-08-31 1987-03-10 Bio-Logic Systems Corp. Brain electrical activity topographical mapping
WO1988010093A1 (fr) * 1987-06-26 1988-12-29 Nicolet Instrument Corporation Procede et systeme pour l'analyse d'enregistrements polygraphiques physiologiques a long terme
US4776345A (en) * 1987-09-04 1988-10-11 Cns, Inc. Interactive determination of sleep stages

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
International Journal of Bio-Medical Computing, Vol. 19, No. 1, July 1986, RAY et al., "Computer sleep stage scoring -- an expert system approach", pages 43-61 (Abstract only provided). *
See also references of EP0505491A4 *

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0705070A1 (fr) * 1993-06-23 1996-04-10 Aequitron Medical, Inc. Evaluation iterative du sommeil
EP0705070A4 (fr) * 1993-06-23 1997-06-11 Aequitron Medical Inc Evaluation iterative du sommeil
DE4339154A1 (de) * 1993-11-16 1995-05-18 Hewlett Packard Gmbh Anästhesie-Protokollsystem und Verfahren zum Steuern desselben
US5560352A (en) * 1993-11-16 1996-10-01 Hewlett-Packard Company Anesthesia protocol system and method of controlling the same
EP0678809A2 (fr) * 1994-04-13 1995-10-25 Becton, Dickinson and Company Dispositif pour l'automatisation du traitement par lots d'analyses de données
EP0678809A3 (fr) * 1994-04-13 1997-07-09 Becton Dickinson Co Dispositif pour l'automatisation du traitement par lots d'analyses de données.
WO1997014354A2 (fr) * 1995-10-16 1997-04-24 MAP Medizintechnik für Arzt und Patient GmbH Procede et dispositif pour l'analyse quantitative de troubles du sommeil
WO1997014354A3 (fr) * 1995-10-16 1997-06-05 Map Gmbh Procede et dispositif pour l'analyse quantitative de troubles du sommeil
US6120441A (en) * 1995-10-16 2000-09-19 Map Medizintechnik Fur Arzt Und Patient Gmbh Method and device for quantitative analysis of sleep disturbances
WO1998006326A1 (fr) * 1996-08-15 1998-02-19 Nellcor Puritan Bennett Incorporated Systemes de controle de patients
AU731448B2 (en) * 1996-08-15 2001-03-29 Nellcor Puritan Bennett Incorporated Patient monitoring system
GB2381586A (en) * 2001-11-01 2003-05-07 Oxford Biosignals Ltd Electro-Oculographic Sleep Monitoring
WO2004028365A2 (fr) * 2002-09-20 2004-04-08 MCC Gesellschaft für Diagnosesysteme in Medizin und Technik mbH & Co. KG Procede et dispositif permettant de determiner un profil de sommeil
WO2004028365A3 (fr) * 2002-09-20 2004-06-03 Mcc Ges Fuer Diagnosesysteme I Procede et dispositif permettant de determiner un profil de sommeil
EP2589335A3 (fr) * 2003-04-10 2017-10-04 Adidas AG Systèmes et procédés de détection d'événements respiratoires
US7170994B2 (en) 2003-10-15 2007-01-30 Motorola, Inc. Method and apparatus for selecting an alert mode based on user biometrics
US8364254B2 (en) 2009-01-28 2013-01-29 Brainscope Company, Inc. Method and device for probabilistic objective assessment of brain function
US10321840B2 (en) 2009-08-14 2019-06-18 Brainscope Company, Inc. Development of fully-automated classifier builders for neurodiagnostic applications
WO2011084394A1 (fr) * 2009-12-16 2011-07-14 Brainscope Company, Inc. Méthode et dispositif pour l'évaluation neurologique d'intervention et le guidage du traitement
US9538949B2 (en) 2010-09-28 2017-01-10 Masimo Corporation Depth of consciousness monitor including oximeter
US9775545B2 (en) 2010-09-28 2017-10-03 Masimo Corporation Magnetic electrical connector for patient monitors
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US11717210B2 (en) 2010-09-28 2023-08-08 Masimo Corporation Depth of consciousness monitor including oximeter
US10154815B2 (en) 2014-10-07 2018-12-18 Masimo Corporation Modular physiological sensors
US10765367B2 (en) 2014-10-07 2020-09-08 Masimo Corporation Modular physiological sensors
US11717218B2 (en) 2014-10-07 2023-08-08 Masimo Corporation Modular physiological sensor

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Publication number Publication date
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EP0505491A1 (fr) 1992-09-30
EP0505491A4 (en) 1993-09-01

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