CA1054262A - Nuclear stethoscope - Google Patents
Nuclear stethoscopeInfo
- Publication number
- CA1054262A CA1054262A CA247,374A CA247374A CA1054262A CA 1054262 A CA1054262 A CA 1054262A CA 247374 A CA247374 A CA 247374A CA 1054262 A CA1054262 A CA 1054262A
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- CA
- Canada
- Prior art keywords
- memory
- channel
- channels
- producing
- heart
- 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.)
- Expired
Links
- 230000000747 cardiac effect Effects 0.000 claims abstract description 27
- 239000008280 blood Substances 0.000 claims abstract description 19
- 210000004369 blood Anatomy 0.000 claims abstract description 19
- 230000001186 cumulative effect Effects 0.000 claims abstract description 13
- 239000000700 radioactive tracer Substances 0.000 claims abstract description 6
- 230000000875 corresponding effect Effects 0.000 claims description 20
- 230000005855 radiation Effects 0.000 claims description 14
- 230000001360 synchronised effect Effects 0.000 claims description 4
- 239000002131 composite material Substances 0.000 claims description 3
- 230000001276 controlling effect Effects 0.000 claims description 3
- 238000002955 isolation Methods 0.000 claims description 3
- 230000029058 respiratory gaseous exchange Effects 0.000 claims description 2
- 238000005070 sampling Methods 0.000 claims 12
- 239000000126 substance Substances 0.000 claims 2
- 238000001914 filtration Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000012163 sequencing technique Methods 0.000 claims 1
- 239000000523 sample Substances 0.000 description 7
- 230000006870 function Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 230000002285 radioactive effect Effects 0.000 description 4
- 230000017531 blood circulation Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000000718 qrs complex Methods 0.000 description 3
- 238000001514 detection method Methods 0.000 description 2
- 238000003745 diagnosis Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000005251 gamma ray Effects 0.000 description 2
- 210000005240 left ventricle Anatomy 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 230000001960 triggered effect Effects 0.000 description 2
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- GKLVYJBZJHMRIY-OUBTZVSYSA-N Technetium-99 Chemical compound [99Tc] GKLVYJBZJHMRIY-OUBTZVSYSA-N 0.000 description 1
- 238000013155 cardiography Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000012631 diagnostic technique Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 210000000554 iris Anatomy 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000009206 nuclear medicine Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940056501 technetium 99m Drugs 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 238000012285 ultrasound imaging Methods 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/40—Arrangements for generating radiation specially adapted for radiation diagnosis
- A61B6/4057—Arrangements for generating radiation specially adapted for radiation diagnosis by using radiation sources located in the interior of the body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/02—Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
- A61B5/026—Measuring blood flow
- A61B5/0275—Measuring blood flow using tracers, e.g. dye dilution
- A61B5/02755—Radioactive tracers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
- A61B5/316—Modalities, i.e. specific diagnostic methods
- A61B5/318—Heart-related electrical modalities, e.g. electrocardiography [ECG]
- A61B5/346—Analysis of electrocardiograms
- A61B5/349—Detecting specific parameters of the electrocardiograph cycle
- A61B5/352—Detecting R peaks, e.g. for synchronising diagnostic apparatus; Estimating R-R interval
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/74—Details of notification to user or communication with user or patient ; user input means
- A61B5/7475—User input or interface means, e.g. keyboard, pointing device, joystick
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/42—Arrangements for detecting radiation specially adapted for radiation diagnosis
- A61B6/4208—Arrangements for detecting radiation specially adapted for radiation diagnosis characterised by using a particular type of detector
- A61B6/4258—Arrangements for detecting radiation specially adapted for radiation diagnosis characterised by using a particular type of detector for detecting non x-ray radiation, e.g. gamma radiation
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01T—MEASUREMENT OF NUCLEAR OR X-RADIATION
- G01T1/00—Measuring X-radiation, gamma radiation, corpuscular radiation, or cosmic radiation
- G01T1/16—Measuring radiation intensity
- G01T1/161—Applications in the field of nuclear medicine, e.g. in vivo counting
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/50—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment specially adapted for specific body parts; specially adapted for specific clinical applications
- A61B6/507—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment specially adapted for specific body parts; specially adapted for specific clinical applications for determination of haemodynamic parameters, e.g. perfusion CT
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medical Informatics (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Animal Behavior & Ethology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pathology (AREA)
- Surgery (AREA)
- Biophysics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Cardiology (AREA)
- High Energy & Nuclear Physics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Optics & Photonics (AREA)
- Radiology & Medical Imaging (AREA)
- Physiology (AREA)
- General Physics & Mathematics (AREA)
- Hematology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Nuclear Medicine (AREA)
- Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
Abstract
NUCLEAR STETHOSCOPE A built-up image illustrating blood volume in the heart versus time taken over many cardiac cycles is produced by continuously displaying a graph of cumulative data indicating the amount of radioactivity from a tracer in the blood detected in the heart during each of a series of intervals into which the average cardiac period is divided. The parallel lines of a raster scan display correspond respectively to the memory channels. The count stored in a particular memory channel causes the video signal for the corresponding line to be maintained at a binary level for a corresponding time interval thus generating a bar graph in which the length of each bar indicates the amount of radioactivity sensed during the corresponding interval of the cardiac cycle. As each memory channel accumulates radioactivity data with each successive cardiac cycle, each bar displayed in the bar graph lengthens to indicate the cumulative activity until an interpretable curve is obtained.
Description
sackground of the Invention The invention relates generally to the fiel~ of nuclear medicine and, more specifically, to diagnostic techniques of analyzing blood flow through the heart by detecting radioactivity fro~ radioisotopes injected into the bloodstream.
In addition to the standard tools of cardiac diagnosis, the electrocardiogram (ECG) and the conventional stethoscope for audible heart sounds, relatively new techni~ues including angiograms, ultrasound cardiography and the measure-ment of radioactivity in the blood are being investigated and implemented to increase the amount of quantitative data to provide a more reliable basis for diagnosis. In ascertaining the efficiency of the heart, it is desirable to determine the A
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volumetric rate of flow of blood through the heart. ~or example, the difference in volume of the left ventricle during different phases of the cardiac cycle is indicative of the rate of blood ~low.
Volumetric measurements can be approximated by using X-ray or ultrasound imaging techniques. Ano~her type of X-ray technique is shown in U.S. Patent No. 3,824,399 to Bjork et al, July 16, 1974 which indicates the concentration of an X-ray opaque - tracer in the heart over a period of several cardiac cycles to generate quantitative data concerning the rate of blood flow.
The same type of techni~ue was earlier employed by injeeting a radioisotope into the blood stream entering the heart and using a scintillation detector or Geiger counter to determine the varia-tions in concentration of the radioactive tracer in the outflow tract of the heart over several cardiac cycles. The collected data was plotted and used to determine the rate of blood flow through the heart. See, for example, U.S. Patent Nos. 3,221,731 to Annis et al, December 7, 1965 and 3,528,407 to Espagno et al, September 15, 1970.
Prior systems utilizing detection of radioisotope concentration to analyze the rate of ~ow of blood have been deficient in providing data quickly to the physician in a readily interpretable format.
Summary of the Invention The general purpose of the present invention is to generate a readily interpretable display of radiation (or gamma radiation) emitted from the heart blood pool at precise points in the cardiac cycle with the data for each point accumulated over many heart beats and displayed in one composite image showing the integrated activity at points within the cardiac cycle. A collimated probe aimed at a selected location in the heart detects the concentration of radioactive isotope in the blood by producing output pulses which are counted and stored over a brief repeating interval of time in a multichannel memory. A first channel of memory is gated by detection of the QRS complex in the patient's ECG. Thereafter, the channels of memory are successively addressed so that each successive radiation count over repeating time intervals will be stored in a corresponding memory channel. With the subsequent heart beat, the process is reiterated and a new count is added to the count that is already in storage for a particular channel.
Simultaneously, the memory channels are read out to a TV type display in which each memory channel is correlated with ' 15 a "horizontal" line sweep. At the beginning of each line, the video input signal is switched from a low level to a high level where it remains for a period of time which corresponds to the accumulated total in the memory chaNnels thus writing a line on the TV screen whose length is determined by the accumulated ~20 radioactivity counts.
Since successive lines of the display correspond to different points of the cardiac cycle, the physician can observe the build-up of an image over a period of about a minute which will illustrate the variation in concentration of radioactive isotope at that selected part of the heart blood pool during the patient's cardiac cycle. The same instrument is designed to operate in a "dynamic" mode, instead of being synchronized to the ECG, in which a nonreiterated (one-pass) test is per-formed by accumulating a radioactivity count over a longer .
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., - ~
~os4z62 period of time (e.g., 100 milliseconds) at each channel before the memory input is switched to the next channel.
Brief Descri tion of the Drawings P
Fig. 1 is a front view of an instrument including a control panel and display screen with a pictorial representation of a typical image produced according to the present invention;
and Fig. 2 is a block diagram illustrating the electronics associated with the instrument of Fig. 1.
Description of the Preferred Embodiment The instrument illustrated in Figs. 1 and 2 and des-cribed below is designed to permit immediate visualization of the time-activity curve of a radioactive isotope carried in the blood within the patient's heart. The mstrument has two modes of operation termed the "SYNC" and "DYNAMIC" modes. The block diagram in Fig. 2 illustrates all of the functional elements of the electronic system for operating in either mode.
The term SYNC mode is used because the storage of information is synchronized to the patient's ECG R-wave (center peak of the QRS complex). The storage interval for each memory channel as explained below is made short enough that a desired number of intervals can be sampled during each cardiac cycle.
The synchronization aspect is manifested by the fact that the counter, which increments the channel destination or address for incoming data, is reset with each R-wave to "recycle" the memory channels. Thè SYNC mode can continue indefinitely until switched OFF, although it is effectively finished (and worthless for displaying) when all of the channels have been written com-pletely full so that the memory is no longer registering new data.
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In contrast, the DYNP~lIC mode makes only a single pass through all of the memory channels with each channel being "open" for a much longer interval than in the SYNC mode. After the radioactivity in the final interval (last channel) has been S counted, the DYNAMIC mode is automatically terminated.
The following detailed discussion wlll begin with a treatment of the system in the SYNC mode leaving certain control aspects to be explained at the end, such as how the DYNAMIC and SYNC modes are selected and initiated.
In Fig. 2 the patient's ECG signal is amplified and filtered to reject respiration, myogram, and other noise~in the ECG isolation amplifier 10 and the QRS complex is discrimi-nated by a conventional QRS detector 12 with front panel indi-cator light 12a (Fig. 1) to provide a reset signal for the memory channel switching system described below. A collimated probe 14, powered by an adjustable high voltage DC power supply 16 (typically 300-1000 volts DC), consists of a NaI crystal (typically 1 1/2 inches in diameter), a photomultiplier tube and a shielded, deep-focus collimator with two irises, which yield an "icepick" or pinhole field of view. A gamma ray from the focal point of the probe 14, manually positioned in the heart blood pool, causes a current pulse from the probe 14 which is passed via a nuclear pulse amplifier 18 to a single channel analyzer 20. The analyzer 20 produces a digital output pulse signifying the receipt of a valid gamma ray, as evidenced by the output of the amplifier being between certain voltage limits. Note that the term "single channel" refers only to the fact that one kind of radiation is being detected and has nothing to do with the term multichannel memory used to designate ,, ,:
the plurality of memory channels corresponding to adjacent intervals in the cardiac cycle.
A variable range ratemeter circuit 22 converts the l pulse rate from the analyzer 20 to a voltage which drives theS count ratemeter 24 to indicate whether the power supply 16 must be adjusted with knob 16a (Fig. 1), controlling the photo-multiplier gain, to accommodate the particular isotope being used. The front panel switch 22a (Fig. 1) changes the range of the count ratemeter 22 by a factor of 100, 1000, or 10,000.
The digital pulse output of the analyzer 20 is simul-taneously passed to the counter 26 which counts one "nuclear .
event" each time it receives a pulse from the output of the analyzer 20. In order to count the number of events in adjacent l~ ~ intervals within a span of a single cardiac cycle, the nuclear ;' 15 event counter is reset to zero (cleared) at the beginning of each interval by means of an adjustable time-per-channel time base generator 28. In the preferred embodiment, three options are available for the number of channels of memory: 192, 96 or 48, as discussed below. The time base generator 28, in , 20 cooperation with a frequency divider 29 (including multipliers if necessary), issues a clock pulse nominally every 5.12 milli-, seconds, 10.24 milliseconds or 20.48 milliseconds, as a function of the number of channels selected to provide coverage of the - entire cardiac cycle at the approximate heart rate of 60 beats per minute. The nominal setting can be varied over a 4:1 range ; centered on the nominal setting via the front panel max./min.
rate control knob 28a to accommodate the patient's heart rate, that is, to insure that all 192 channels, for instance, are : ~ being used.
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The output of the nuclear event counter 26 is passed to a multichannel cumulative memory unit 30 including a two-input dlgital adder 32 and an addressable read/write memory 34 with nondestructive readout having 192 channels with 12 bits ~ 5 of storage per channel. The type of memory selected should be ,~ one which is capable of simultaneous write-in and readout of data, for example, a core storage matrix. The nuclear event counter 26 provides one of the inputs (A) to the adder 32. The other input (B) is provided by the data output of the memory 34.
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The output of the adder 32 forms the data input to the memory 34.
The memory is addressed by means of an input channel counter 36 which is reset (i.e., restarted) by the output of the QRS detector 12 via a mode switch 38 and clocked (incre-mented or decremented) by the time base generator 28. During each counting interval (e.g., 5.12 milliseconds) the memory 34 will be storing new cumulative data in a corresponding . ~ .
~channel. In the next time interval, the input channel counter 36 readdresses the memory 34 to a corresponding memory channel.
~ ~ - The memory 34 is thus operated in a cumulative fashion by com-bining the count for a particular interval with the count already stored in the corresponding channel of the memory for all prior-corresponding intervals since starting the SYNC mode.
For the storage (input) opera*ion, the address for the r 25 memory data output which is fed around to the digital adder 32 is controlled by the input channel counter 36 in the same manner as the input address is controlled.
~ In operation, the memory may be addressed by the input ; , channel counter 36 very briefly once per time interval. For i -", l~S4Z~Z
example, at the end of a given time interval, the memory address control is switched from the video section (explained below) to the input channel counter 36 so that the corresponding memory channel is held open for a brief interval of time during which the adder 32 is clocked just before the reset pulse from the time-per-channel time base generator 28 enabling the adder to sum the prior number in the memory channel at the output regis-ter and the count for the current interval and pass the summed count back into the same memory channel. After completion of the updating operation, control of the memory address is switched back to the video display system.
The video section of the instrument services to display ; the updated contents of the memory channels all at once. The memory channels are visually represented by the display in the - form of contiguous parallel lines with the number in each channel being represented by the length of a bar drawn on the line like the construction of a bar graph. Since the channels represent adjacent intervals of time, the disFlay can be represented by an X-Y display where the X-axis represents time and the Y-axis represents radioactivity. The full extent of the X-axis corre-sponds to a single cardiac cycle and the displayed data represents the variation in radioactivity within the cardiac cycle. As the image is built up over a number of cardiac cycles, the displayed data tends to represent the variation in radioactivity within a typical or average cardiac cycle.
The heart of the video section of the instrument is a conventional cathode ray (CRT) tube display 40 shown schematically in Fig. 2 and in front screen view of Fig. 1. A video display time base generator 42 provides appropriately timed SYNC pulses lOS4Z62 to the TV sweep circuits 44 such that horizontal and vertical deflection control signals are generated to produce a conven-tional raster scan pattern of the electron beam on the display 40. The raster pattern is oriented orthogonally relative to a conventional TV raster scan. That is, the lines run vertically.
This is accomplished by rotating the TV monitor by 90. The number of lines in the raster pattern can be determined roughly on a 1:1 relationship with the highest number of memory channels desired. However, there is no reason why the standard composite TV SYNC signal arrangement cannot be used, in which case 525 lines would be produced. If this number of lines were far greater than the number of channels employed, one channel would have to be represented by several adjacent lines to maintain suitable image size.
Besides controlling the generation of the raster pattern on the display 40, the video time base generator 42 also controls the readout function of the multichannel memory 34 at all times except those times at the end of one of the counting time intervals when the memory is updated with new cumulative data. The multiplexing of the address control is accomplished by means of a fast electronic switch 46 which is operated by the time-per-channel time base generator 28. At only one time during each counting time interval is the address controlled by the input channel counter 36. During this subinterval of time, the "update period", the corresponding memory channel is non-destructively interrogated along with the count of the nuclear event counter 26 and the two data are added together and run ' back into the corresponding memory channel. Outside the update period, the digital adder 32, i.e., the data input to the memory ., .
} _g_ 34, is disabled. Following the update period, control of the address of the memory output is returned by means of the switch 46 to the video time base generator 42. The update period is designed to be so brief that it does not inter~ere with the display of the stored information.
The video time base generator 42 causes the output channel address of the memory 34 to be incremented or decremen-ted at the same rate as the line SYNC signals so that each channel's contents will appear at the output simultaneously with each SYNC pulse which starts a line sweep deflection sig-nal. The output register of the memory 34 is connected to one input of a comparator 48. The other input is interconnected with the video time base generator 42. The output of the comparator 48 produces the data video signal which causes a bar to be drawn on the corresponding line of the display with a length that is proportional to the number stored in the corresponding memory channel.
The comparator 48 can be implemented with digital or analog circuitry (not shown). The digital implementation re-quires a fast clock, which is ordinarily available in the form of the time base from which the video time base SYNC signals are generated. The fast clock operates a counter which is triggered or enabled by a line SYNC pulse. A standard digital comparator circuit receives in parallel the outputs of the memory channel and the continually incrementing output of the counter operated by the fast clock. When the count reaches the same number as in the input register for the memory 34, the digital comparator switches from one binary level to the other binary level.
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Exactly the same comparing operation can be done in analog version by using a ramp generator triggered by a line SYNC pulse. The output of the ramp generator would form one input to a differential amplifier, or other comparing circuit, and the other input would be the output of a digital-to-analog converter connected to the memory output register. Both the digital and the analog implementation of the comparator 48 are considered to be strictly conventional for the stated function.
The digital output of the comparator 48 is thus syn-chronized with the lines of display 40. The data level of the video output (i.e., full white) is ON from the beginning of the line up to the point where the comparator 48 finds agreement between the memory channel contents and the reference ramp or count.
The highest useful number that can be contained in a given channel is deemed to be that indicated by a "l" in all 12 bits, which is equivalent in decimal number form to 4,095.
- ~ The steepness of the analog ramp or the rate of the digital reference count used by the comparator 48 should be adjusted so that a full count (4,095) does not exceed the full "width"
of the screen. However, since only a portion of the memory capacity may be used in a given test, it may be necessary to scale the count upward. This is accomplished by the counts per line control 50 in Fig. 2 which is operated by the calibrated ' ~ 25 "counts full scale" knob 50a on the front panel in Fig. l. One way that this scaling up of the data can be accomplished is to take the binary number in the output register of the memory 34 , and shift it one or more "more significant digits" (like moving the decimal point), before entering the number into the comparator 1054Z~2 48. This type of operation is suggested by the powers of 2 calibrations on the counts full scale knob 50a in Fig. 1.
A preferred feature of this instrument is a self-generated grid which allows quantitative measurements of the variation in radioactivity to be measured without regard to non-linearity distortion. For this purpose, a gradicule generator 52 is operated by the same video time base generator 42 which operates the TV sweep circuits. The gradicule genera-tor simply consists of clocked logic circuitry which writes equally spaced white dots along each line sweep to create vertical lines and a full line "white" every nth line to make the horizontal lines of the grid pattern. The video output of the gradicule generator 52 is passed along with the output of the comparator 48 to an EXCLUSIVE OR gate 54 which normally ; 15 passes whichever one o the video outputs is "white". However, when both of the video outputs are white, the EXCLUSIVE OR gate is inhibited. The effect of this logical operation is to cause the lines of the grid to show up as black lines where they would run through the solid portion of the radioactivity curve so that they will be visible at all times as either white lines against a black background or black lines against a white background.
In normal operation the number of channels corre-sponds on a 1:1 basis with the number of lines available for viewing in the display. If desired, however, the number of channels may be selectively reduced. In the preferred embodi-ment, a channel number selector 56 operated by the three-position switch 56a on the front panel of Fig. 1 can be used to divide the number of channels by either 2 or 4 resulting in either 96 or 48 channels, respectively. While none of the radioactivity will be "missed" or not counted when the number of channels is halved, the resolution of the instrument is reduced. If 96 channels is-selected, for example, instead of the full 192, the channel number selector 56 simply cuts out 50% of the memory channels. One way in which this can be accomplished is by using a presettable down counter for the input channel counter 36 where the preset number in the full channel case will be 192 (in decimal form) while in the half channels case, the number will be preset to only 96. In either case when the channel count cQmes down to zero, the counter 36 stops until commanded by the next R-wave to start counting down again from the preset number. At the same time, the channel number selec-tor 56 can be used via the frequency divider 29 to double or quadruple the time lnterval clocked by the time-per-channel time base generator 28. At the same time, the channel number selec-tor 56 must also correct the comparator 48 which produces the vldeo bars. Accordingly, each memory channel is interrogated for two lines or four lines so that two or four equal length-contiguous, parallel bars are written.
Another way to make the video display come out full screen even though the number of channels is divided by two or four would be to connect the memory channels in tandem or in groups of four depending on the setting of the channel number selector 56. For the first address, for example 96, the same data will be entered into two adjacent channels which would normally correspond, for example, to channels 192 and 191. In this way, the video display can read out the channels at the same rate as if the full channel capacity of the memory were being used.
The remaining functions provided on the front panel of the instrument are "SYNC", "DYNAMIC", and "ERASE". The erase control 58 (Fig. 2) operates in a conventional manner to clear the entire memory on command by resetting all 2,304 bits to zero.
The SYNC/DYNAMIC mode control unit 60, operated by means of the SYNC and DYNAMIC push buttons 6Oa and 6Ob on the front panel, has several functions. If the SYNC mode is desired, pushing the SYNC button (e.g., a bistable electro mechanical switch) causes the storage operation to begin with the next R-wave from the patient. Thus, the mode control 60 could be implemented by means of a gated flip-flop where the data input is represented by the position of the SYNC swltch and the output of the QRS detector 12 is the clock pulse which sets the output of the flip-flop to enable the memory to receive data. Thus, once the SYNC switch is set, the SYNC mode of operation will continue indefinitely until the memory capacity is exhausted or until the SYNC switch is repositioned whereupon the SYNC
mode will terminate on the next R-waveO The display will con-tinue to be built up, if permitted, until the entlre screen is white.
If the DYNAMIC (single-pass) mode of operation is desired, the patient's R-wave is of no interest. Thus, throwing the DYNAMIC switch 60b causes the mode switch 38 to open the connection between QRS detector 12 and the reset (preset enable) input of the channel counter 36. Instead of being initiated by the patient's R-wave, the channel counter 36 is reset by actua-tion of the DYNAMIC switch. In addition, selecting the DYNAMIC
mode of operation instantaneously enables the memory 34 and via the frequency divider 29 (or equivalent circuitry) changes the counting interval timed by the channel time base generator 28 to a much longer interval on the order of 100 milliseconds in-stead of 5.12 milliseconds. One hundred ninety-two 100 milli-second intervals results in a 19.2 second study which is auto-matically terminated by virtue of the fact that the channel counter 36 is not reset after it counts 192 channels.
In use, the portable instrument is brought to the bed-side and the patient is typically prepared by injecting albumin containing a radioactive isotope, for example up to 30 milli-curies of technetium-99m, directly into the bloodstream entering the heart and the connections for the ECG unit are made. About ten minutes after injection of the tracer, the physician holds the probe 14 (Fig. 2~ over the patient's precordium and, ob--serving the count ratemeter, locates the focal point in the heart blood pool (e.g., the left ventricle). Once the probe is located, the SYNC button is actuated and the image observed for about a minute until an interpretable curve is obtained.
If during image build-up, the physician feels that a change in the number of channels is in order, the instrument is taken out of SYNC mode, the memory erased, adjustments made and the SYNC mode restarted. The SYNC mode can be interrupted and restarted, if desired, without erasure.
The above detailed description is not intended to restrict the invention as claimed below to any particular form where equivalent implementations exist to carry out the recited function. For example, the collimated probe 14 and nuclear pulse amplifier 18 represent only one way of detecting or sensing radioactivity from a particular point in the heart blood pool ~os~z~z and any other available technique for detecting radiation may be substituted. Moreover, other X-Y display techniques can be substituted for the TV video display of the preferred embodi-ment. Rather, the description is intended to be merely S illustrative of a preferred embodiment of the invention designed to meet certain criteria and specifications which to some degree depend on the specific application and environment in which the instrument will be used. Accordingly, all variations within the range of equivalence are intended to be embraced by the claims which follow.
In addition to the standard tools of cardiac diagnosis, the electrocardiogram (ECG) and the conventional stethoscope for audible heart sounds, relatively new techni~ues including angiograms, ultrasound cardiography and the measure-ment of radioactivity in the blood are being investigated and implemented to increase the amount of quantitative data to provide a more reliable basis for diagnosis. In ascertaining the efficiency of the heart, it is desirable to determine the A
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.. :
.. ... ..
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volumetric rate of flow of blood through the heart. ~or example, the difference in volume of the left ventricle during different phases of the cardiac cycle is indicative of the rate of blood ~low.
Volumetric measurements can be approximated by using X-ray or ultrasound imaging techniques. Ano~her type of X-ray technique is shown in U.S. Patent No. 3,824,399 to Bjork et al, July 16, 1974 which indicates the concentration of an X-ray opaque - tracer in the heart over a period of several cardiac cycles to generate quantitative data concerning the rate of blood flow.
The same type of techni~ue was earlier employed by injeeting a radioisotope into the blood stream entering the heart and using a scintillation detector or Geiger counter to determine the varia-tions in concentration of the radioactive tracer in the outflow tract of the heart over several cardiac cycles. The collected data was plotted and used to determine the rate of blood flow through the heart. See, for example, U.S. Patent Nos. 3,221,731 to Annis et al, December 7, 1965 and 3,528,407 to Espagno et al, September 15, 1970.
Prior systems utilizing detection of radioisotope concentration to analyze the rate of ~ow of blood have been deficient in providing data quickly to the physician in a readily interpretable format.
Summary of the Invention The general purpose of the present invention is to generate a readily interpretable display of radiation (or gamma radiation) emitted from the heart blood pool at precise points in the cardiac cycle with the data for each point accumulated over many heart beats and displayed in one composite image showing the integrated activity at points within the cardiac cycle. A collimated probe aimed at a selected location in the heart detects the concentration of radioactive isotope in the blood by producing output pulses which are counted and stored over a brief repeating interval of time in a multichannel memory. A first channel of memory is gated by detection of the QRS complex in the patient's ECG. Thereafter, the channels of memory are successively addressed so that each successive radiation count over repeating time intervals will be stored in a corresponding memory channel. With the subsequent heart beat, the process is reiterated and a new count is added to the count that is already in storage for a particular channel.
Simultaneously, the memory channels are read out to a TV type display in which each memory channel is correlated with ' 15 a "horizontal" line sweep. At the beginning of each line, the video input signal is switched from a low level to a high level where it remains for a period of time which corresponds to the accumulated total in the memory chaNnels thus writing a line on the TV screen whose length is determined by the accumulated ~20 radioactivity counts.
Since successive lines of the display correspond to different points of the cardiac cycle, the physician can observe the build-up of an image over a period of about a minute which will illustrate the variation in concentration of radioactive isotope at that selected part of the heart blood pool during the patient's cardiac cycle. The same instrument is designed to operate in a "dynamic" mode, instead of being synchronized to the ECG, in which a nonreiterated (one-pass) test is per-formed by accumulating a radioactivity count over a longer .
,.;
., - ~
~os4z62 period of time (e.g., 100 milliseconds) at each channel before the memory input is switched to the next channel.
Brief Descri tion of the Drawings P
Fig. 1 is a front view of an instrument including a control panel and display screen with a pictorial representation of a typical image produced according to the present invention;
and Fig. 2 is a block diagram illustrating the electronics associated with the instrument of Fig. 1.
Description of the Preferred Embodiment The instrument illustrated in Figs. 1 and 2 and des-cribed below is designed to permit immediate visualization of the time-activity curve of a radioactive isotope carried in the blood within the patient's heart. The mstrument has two modes of operation termed the "SYNC" and "DYNAMIC" modes. The block diagram in Fig. 2 illustrates all of the functional elements of the electronic system for operating in either mode.
The term SYNC mode is used because the storage of information is synchronized to the patient's ECG R-wave (center peak of the QRS complex). The storage interval for each memory channel as explained below is made short enough that a desired number of intervals can be sampled during each cardiac cycle.
The synchronization aspect is manifested by the fact that the counter, which increments the channel destination or address for incoming data, is reset with each R-wave to "recycle" the memory channels. Thè SYNC mode can continue indefinitely until switched OFF, although it is effectively finished (and worthless for displaying) when all of the channels have been written com-pletely full so that the memory is no longer registering new data.
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In contrast, the DYNP~lIC mode makes only a single pass through all of the memory channels with each channel being "open" for a much longer interval than in the SYNC mode. After the radioactivity in the final interval (last channel) has been S counted, the DYNAMIC mode is automatically terminated.
The following detailed discussion wlll begin with a treatment of the system in the SYNC mode leaving certain control aspects to be explained at the end, such as how the DYNAMIC and SYNC modes are selected and initiated.
In Fig. 2 the patient's ECG signal is amplified and filtered to reject respiration, myogram, and other noise~in the ECG isolation amplifier 10 and the QRS complex is discrimi-nated by a conventional QRS detector 12 with front panel indi-cator light 12a (Fig. 1) to provide a reset signal for the memory channel switching system described below. A collimated probe 14, powered by an adjustable high voltage DC power supply 16 (typically 300-1000 volts DC), consists of a NaI crystal (typically 1 1/2 inches in diameter), a photomultiplier tube and a shielded, deep-focus collimator with two irises, which yield an "icepick" or pinhole field of view. A gamma ray from the focal point of the probe 14, manually positioned in the heart blood pool, causes a current pulse from the probe 14 which is passed via a nuclear pulse amplifier 18 to a single channel analyzer 20. The analyzer 20 produces a digital output pulse signifying the receipt of a valid gamma ray, as evidenced by the output of the amplifier being between certain voltage limits. Note that the term "single channel" refers only to the fact that one kind of radiation is being detected and has nothing to do with the term multichannel memory used to designate ,, ,:
the plurality of memory channels corresponding to adjacent intervals in the cardiac cycle.
A variable range ratemeter circuit 22 converts the l pulse rate from the analyzer 20 to a voltage which drives theS count ratemeter 24 to indicate whether the power supply 16 must be adjusted with knob 16a (Fig. 1), controlling the photo-multiplier gain, to accommodate the particular isotope being used. The front panel switch 22a (Fig. 1) changes the range of the count ratemeter 22 by a factor of 100, 1000, or 10,000.
The digital pulse output of the analyzer 20 is simul-taneously passed to the counter 26 which counts one "nuclear .
event" each time it receives a pulse from the output of the analyzer 20. In order to count the number of events in adjacent l~ ~ intervals within a span of a single cardiac cycle, the nuclear ;' 15 event counter is reset to zero (cleared) at the beginning of each interval by means of an adjustable time-per-channel time base generator 28. In the preferred embodiment, three options are available for the number of channels of memory: 192, 96 or 48, as discussed below. The time base generator 28, in , 20 cooperation with a frequency divider 29 (including multipliers if necessary), issues a clock pulse nominally every 5.12 milli-, seconds, 10.24 milliseconds or 20.48 milliseconds, as a function of the number of channels selected to provide coverage of the - entire cardiac cycle at the approximate heart rate of 60 beats per minute. The nominal setting can be varied over a 4:1 range ; centered on the nominal setting via the front panel max./min.
rate control knob 28a to accommodate the patient's heart rate, that is, to insure that all 192 channels, for instance, are : ~ being used.
i' - ~054Z~iZ
The output of the nuclear event counter 26 is passed to a multichannel cumulative memory unit 30 including a two-input dlgital adder 32 and an addressable read/write memory 34 with nondestructive readout having 192 channels with 12 bits ~ 5 of storage per channel. The type of memory selected should be ,~ one which is capable of simultaneous write-in and readout of data, for example, a core storage matrix. The nuclear event counter 26 provides one of the inputs (A) to the adder 32. The other input (B) is provided by the data output of the memory 34.
.
The output of the adder 32 forms the data input to the memory 34.
The memory is addressed by means of an input channel counter 36 which is reset (i.e., restarted) by the output of the QRS detector 12 via a mode switch 38 and clocked (incre-mented or decremented) by the time base generator 28. During each counting interval (e.g., 5.12 milliseconds) the memory 34 will be storing new cumulative data in a corresponding . ~ .
~channel. In the next time interval, the input channel counter 36 readdresses the memory 34 to a corresponding memory channel.
~ ~ - The memory 34 is thus operated in a cumulative fashion by com-bining the count for a particular interval with the count already stored in the corresponding channel of the memory for all prior-corresponding intervals since starting the SYNC mode.
For the storage (input) opera*ion, the address for the r 25 memory data output which is fed around to the digital adder 32 is controlled by the input channel counter 36 in the same manner as the input address is controlled.
~ In operation, the memory may be addressed by the input ; , channel counter 36 very briefly once per time interval. For i -", l~S4Z~Z
example, at the end of a given time interval, the memory address control is switched from the video section (explained below) to the input channel counter 36 so that the corresponding memory channel is held open for a brief interval of time during which the adder 32 is clocked just before the reset pulse from the time-per-channel time base generator 28 enabling the adder to sum the prior number in the memory channel at the output regis-ter and the count for the current interval and pass the summed count back into the same memory channel. After completion of the updating operation, control of the memory address is switched back to the video display system.
The video section of the instrument services to display ; the updated contents of the memory channels all at once. The memory channels are visually represented by the display in the - form of contiguous parallel lines with the number in each channel being represented by the length of a bar drawn on the line like the construction of a bar graph. Since the channels represent adjacent intervals of time, the disFlay can be represented by an X-Y display where the X-axis represents time and the Y-axis represents radioactivity. The full extent of the X-axis corre-sponds to a single cardiac cycle and the displayed data represents the variation in radioactivity within the cardiac cycle. As the image is built up over a number of cardiac cycles, the displayed data tends to represent the variation in radioactivity within a typical or average cardiac cycle.
The heart of the video section of the instrument is a conventional cathode ray (CRT) tube display 40 shown schematically in Fig. 2 and in front screen view of Fig. 1. A video display time base generator 42 provides appropriately timed SYNC pulses lOS4Z62 to the TV sweep circuits 44 such that horizontal and vertical deflection control signals are generated to produce a conven-tional raster scan pattern of the electron beam on the display 40. The raster pattern is oriented orthogonally relative to a conventional TV raster scan. That is, the lines run vertically.
This is accomplished by rotating the TV monitor by 90. The number of lines in the raster pattern can be determined roughly on a 1:1 relationship with the highest number of memory channels desired. However, there is no reason why the standard composite TV SYNC signal arrangement cannot be used, in which case 525 lines would be produced. If this number of lines were far greater than the number of channels employed, one channel would have to be represented by several adjacent lines to maintain suitable image size.
Besides controlling the generation of the raster pattern on the display 40, the video time base generator 42 also controls the readout function of the multichannel memory 34 at all times except those times at the end of one of the counting time intervals when the memory is updated with new cumulative data. The multiplexing of the address control is accomplished by means of a fast electronic switch 46 which is operated by the time-per-channel time base generator 28. At only one time during each counting time interval is the address controlled by the input channel counter 36. During this subinterval of time, the "update period", the corresponding memory channel is non-destructively interrogated along with the count of the nuclear event counter 26 and the two data are added together and run ' back into the corresponding memory channel. Outside the update period, the digital adder 32, i.e., the data input to the memory ., .
} _g_ 34, is disabled. Following the update period, control of the address of the memory output is returned by means of the switch 46 to the video time base generator 42. The update period is designed to be so brief that it does not inter~ere with the display of the stored information.
The video time base generator 42 causes the output channel address of the memory 34 to be incremented or decremen-ted at the same rate as the line SYNC signals so that each channel's contents will appear at the output simultaneously with each SYNC pulse which starts a line sweep deflection sig-nal. The output register of the memory 34 is connected to one input of a comparator 48. The other input is interconnected with the video time base generator 42. The output of the comparator 48 produces the data video signal which causes a bar to be drawn on the corresponding line of the display with a length that is proportional to the number stored in the corresponding memory channel.
The comparator 48 can be implemented with digital or analog circuitry (not shown). The digital implementation re-quires a fast clock, which is ordinarily available in the form of the time base from which the video time base SYNC signals are generated. The fast clock operates a counter which is triggered or enabled by a line SYNC pulse. A standard digital comparator circuit receives in parallel the outputs of the memory channel and the continually incrementing output of the counter operated by the fast clock. When the count reaches the same number as in the input register for the memory 34, the digital comparator switches from one binary level to the other binary level.
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Exactly the same comparing operation can be done in analog version by using a ramp generator triggered by a line SYNC pulse. The output of the ramp generator would form one input to a differential amplifier, or other comparing circuit, and the other input would be the output of a digital-to-analog converter connected to the memory output register. Both the digital and the analog implementation of the comparator 48 are considered to be strictly conventional for the stated function.
The digital output of the comparator 48 is thus syn-chronized with the lines of display 40. The data level of the video output (i.e., full white) is ON from the beginning of the line up to the point where the comparator 48 finds agreement between the memory channel contents and the reference ramp or count.
The highest useful number that can be contained in a given channel is deemed to be that indicated by a "l" in all 12 bits, which is equivalent in decimal number form to 4,095.
- ~ The steepness of the analog ramp or the rate of the digital reference count used by the comparator 48 should be adjusted so that a full count (4,095) does not exceed the full "width"
of the screen. However, since only a portion of the memory capacity may be used in a given test, it may be necessary to scale the count upward. This is accomplished by the counts per line control 50 in Fig. 2 which is operated by the calibrated ' ~ 25 "counts full scale" knob 50a on the front panel in Fig. l. One way that this scaling up of the data can be accomplished is to take the binary number in the output register of the memory 34 , and shift it one or more "more significant digits" (like moving the decimal point), before entering the number into the comparator 1054Z~2 48. This type of operation is suggested by the powers of 2 calibrations on the counts full scale knob 50a in Fig. 1.
A preferred feature of this instrument is a self-generated grid which allows quantitative measurements of the variation in radioactivity to be measured without regard to non-linearity distortion. For this purpose, a gradicule generator 52 is operated by the same video time base generator 42 which operates the TV sweep circuits. The gradicule genera-tor simply consists of clocked logic circuitry which writes equally spaced white dots along each line sweep to create vertical lines and a full line "white" every nth line to make the horizontal lines of the grid pattern. The video output of the gradicule generator 52 is passed along with the output of the comparator 48 to an EXCLUSIVE OR gate 54 which normally ; 15 passes whichever one o the video outputs is "white". However, when both of the video outputs are white, the EXCLUSIVE OR gate is inhibited. The effect of this logical operation is to cause the lines of the grid to show up as black lines where they would run through the solid portion of the radioactivity curve so that they will be visible at all times as either white lines against a black background or black lines against a white background.
In normal operation the number of channels corre-sponds on a 1:1 basis with the number of lines available for viewing in the display. If desired, however, the number of channels may be selectively reduced. In the preferred embodi-ment, a channel number selector 56 operated by the three-position switch 56a on the front panel of Fig. 1 can be used to divide the number of channels by either 2 or 4 resulting in either 96 or 48 channels, respectively. While none of the radioactivity will be "missed" or not counted when the number of channels is halved, the resolution of the instrument is reduced. If 96 channels is-selected, for example, instead of the full 192, the channel number selector 56 simply cuts out 50% of the memory channels. One way in which this can be accomplished is by using a presettable down counter for the input channel counter 36 where the preset number in the full channel case will be 192 (in decimal form) while in the half channels case, the number will be preset to only 96. In either case when the channel count cQmes down to zero, the counter 36 stops until commanded by the next R-wave to start counting down again from the preset number. At the same time, the channel number selec-tor 56 can be used via the frequency divider 29 to double or quadruple the time lnterval clocked by the time-per-channel time base generator 28. At the same time, the channel number selec-tor 56 must also correct the comparator 48 which produces the vldeo bars. Accordingly, each memory channel is interrogated for two lines or four lines so that two or four equal length-contiguous, parallel bars are written.
Another way to make the video display come out full screen even though the number of channels is divided by two or four would be to connect the memory channels in tandem or in groups of four depending on the setting of the channel number selector 56. For the first address, for example 96, the same data will be entered into two adjacent channels which would normally correspond, for example, to channels 192 and 191. In this way, the video display can read out the channels at the same rate as if the full channel capacity of the memory were being used.
The remaining functions provided on the front panel of the instrument are "SYNC", "DYNAMIC", and "ERASE". The erase control 58 (Fig. 2) operates in a conventional manner to clear the entire memory on command by resetting all 2,304 bits to zero.
The SYNC/DYNAMIC mode control unit 60, operated by means of the SYNC and DYNAMIC push buttons 6Oa and 6Ob on the front panel, has several functions. If the SYNC mode is desired, pushing the SYNC button (e.g., a bistable electro mechanical switch) causes the storage operation to begin with the next R-wave from the patient. Thus, the mode control 60 could be implemented by means of a gated flip-flop where the data input is represented by the position of the SYNC swltch and the output of the QRS detector 12 is the clock pulse which sets the output of the flip-flop to enable the memory to receive data. Thus, once the SYNC switch is set, the SYNC mode of operation will continue indefinitely until the memory capacity is exhausted or until the SYNC switch is repositioned whereupon the SYNC
mode will terminate on the next R-waveO The display will con-tinue to be built up, if permitted, until the entlre screen is white.
If the DYNAMIC (single-pass) mode of operation is desired, the patient's R-wave is of no interest. Thus, throwing the DYNAMIC switch 60b causes the mode switch 38 to open the connection between QRS detector 12 and the reset (preset enable) input of the channel counter 36. Instead of being initiated by the patient's R-wave, the channel counter 36 is reset by actua-tion of the DYNAMIC switch. In addition, selecting the DYNAMIC
mode of operation instantaneously enables the memory 34 and via the frequency divider 29 (or equivalent circuitry) changes the counting interval timed by the channel time base generator 28 to a much longer interval on the order of 100 milliseconds in-stead of 5.12 milliseconds. One hundred ninety-two 100 milli-second intervals results in a 19.2 second study which is auto-matically terminated by virtue of the fact that the channel counter 36 is not reset after it counts 192 channels.
In use, the portable instrument is brought to the bed-side and the patient is typically prepared by injecting albumin containing a radioactive isotope, for example up to 30 milli-curies of technetium-99m, directly into the bloodstream entering the heart and the connections for the ECG unit are made. About ten minutes after injection of the tracer, the physician holds the probe 14 (Fig. 2~ over the patient's precordium and, ob--serving the count ratemeter, locates the focal point in the heart blood pool (e.g., the left ventricle). Once the probe is located, the SYNC button is actuated and the image observed for about a minute until an interpretable curve is obtained.
If during image build-up, the physician feels that a change in the number of channels is in order, the instrument is taken out of SYNC mode, the memory erased, adjustments made and the SYNC mode restarted. The SYNC mode can be interrupted and restarted, if desired, without erasure.
The above detailed description is not intended to restrict the invention as claimed below to any particular form where equivalent implementations exist to carry out the recited function. For example, the collimated probe 14 and nuclear pulse amplifier 18 represent only one way of detecting or sensing radioactivity from a particular point in the heart blood pool ~os~z~z and any other available technique for detecting radiation may be substituted. Moreover, other X-Y display techniques can be substituted for the TV video display of the preferred embodi-ment. Rather, the description is intended to be merely S illustrative of a preferred embodiment of the invention designed to meet certain criteria and specifications which to some degree depend on the specific application and environment in which the instrument will be used. Accordingly, all variations within the range of equivalence are intended to be embraced by the claims which follow.
Claims (15)
OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A system for displaying the variation in radioactivity within a patient's cardiac cycle from a tracer substance in the blood comprising: detector means for providing an output indicative of the amount of radiation emitted from a selected location in the heart blood pool; timing means for determining successive sampling intervals; nuclear event integrator means responsive to said timing means and said detector means output for producing an output indicative of the amount of said radiation detected in each successive sampling interval; addressable N
channel cumulative memory means for accumulating a representation of the total amount of radiation indicated by said integrator means for every nth sampling interval in a corresponding one of N memory channels: heart beat responsive means for generating a synchroni-zing pulse at the patient's heart rate; memory channel addressing means responsive to said timing means and said heart beat respons-ive means for incrementing the input channel address for said memory means with each sampling interval in a repeating sequence of N predetermined channel addresses in which each successive sequence is initiated by said synchronizing digital pulse; and means for displaying simultaneously the contents of all N channels of said memory means in the format of N adjacently spaced visible indicia each having a height above a common axis according to the current cumulative total represented in the corresponding memory channels respectively.
channel cumulative memory means for accumulating a representation of the total amount of radiation indicated by said integrator means for every nth sampling interval in a corresponding one of N memory channels: heart beat responsive means for generating a synchroni-zing pulse at the patient's heart rate; memory channel addressing means responsive to said timing means and said heart beat respons-ive means for incrementing the input channel address for said memory means with each sampling interval in a repeating sequence of N predetermined channel addresses in which each successive sequence is initiated by said synchronizing digital pulse; and means for displaying simultaneously the contents of all N channels of said memory means in the format of N adjacently spaced visible indicia each having a height above a common axis according to the current cumulative total represented in the corresponding memory channels respectively.
2. The system of claim 1, wherein said displaying means includes means for producing said visible indicia in the form of N adjacent parallel lines each having lengths corresponding to the cumulative total represented in the corresponding memory channels respectively.
3. The system of claim 1, wherein said detector means includes transducer means for producing output pulses indicative of radiation emitted from a selected location in the heart blood pool, and analyzer means responsive to the output pulses of said transducer means for producing a digital pulse output indicative of a particular kind of radiation; and said integrator means includes a nuclear event counter means for counting the number of digital pulses in each successive sampling interval.
4. The system of claim 1, wherein said memory means includes an N channel addressable read/write digital memory and two-input adder means having one input connected to the memory readout and the other input connected to the nuclear event integrator means for producing the sum of the two inputs as the data input to said memory for providing a cumulative total in said memory of the output of said nuclear event integrator means.
5. The system of claim 1, wherein said displaying means includes a video display, means for generating a raster scan in said display comprising a sequence of at least N adjacent line sweeps, and comparator means synchronized with said raster scan for generating a digital data video signal beginning approximately at the start of each line sweep and terminating during the line sweep after an interval corresponding to the cumulative total in the corresponding memory channel of said memory means to produce a composite data image on said video display.
6. The system of claim 5, wherein said comparator means includes means for interrogating the channels of said memory means at the rate of said raster scan.
7. The system of claim 5, wherein said displaying means further includes means for generating a digital gradicule video signal to produce a grid pattern of lines on said display, and EXCLUSIVE OR means for gating said data and gradicule video signals to said display such that coincidence of the two signals results in reduced video signal so that the grid pattern is not obscured by said data image.
8. The system of claim 1, further comprising means for adjusting said sampling interval over a predetermined range to allot N consecutive sampling intervals to the patient's cardiac period.
9. The system of claim 1, further comprising means for selectively dividing the number of memory channels in said memory means and correspondingly lengthening the sampling interval to lower the resolution of the display.
10. The system of claim 1, further comprising means for disconnecting said memory channel addressing means from said synchronizing pulse and for sequencing said memory means once through said N channels on command.
11. A system for displaying the variation in radioactivity within a patient's cardiac cycle from a tracer substance within the blood comprising:
detector means for providing an output indication of the amount of radiation emitted from a selected location in the patient's heart blood pool, timing means for determining a plurality of correspond-ing sampling intervals in each of a plurality of cardiac cycles, adding means connected with the detector means and the timing means for summing over a plurality of cardiac cycles the amount of radiation emitted from said selected location in each corresponding sampling interval, means connected with the adding means for producing an indication of the cumulative amount of radiation emitted in each of the corresponding sampling intervals all at once.
detector means for providing an output indication of the amount of radiation emitted from a selected location in the patient's heart blood pool, timing means for determining a plurality of correspond-ing sampling intervals in each of a plurality of cardiac cycles, adding means connected with the detector means and the timing means for summing over a plurality of cardiac cycles the amount of radiation emitted from said selected location in each corresponding sampling interval, means connected with the adding means for producing an indication of the cumulative amount of radiation emitted in each of the corresponding sampling intervals all at once.
12. The system as set forth in claim 11 further including a memory having a plurality of channels operatively connected with the adding means, whereby the adding means adds to each channel the amount of radiation emitted from said selected location in each corresponding sampling interval over a plurality of cardiac cycles, and wherein the indication producing means is connected to said memory for displaying the cumulative amounts in each channel.
13. The system as set forth in claim 12 further including channel counter means for periodically addressing individual ones of the plurality of channels in each cardiac cycle.
14. The system as set forth in claim 13 wherein the timing means includes EKG signal production means connected with the patient for producing the patient EKG signal, an EKG isolation amplifier for amplifying and filtering the EKG signal for rejecting respiration, myogram and other noise, a detector connected to the EKG isolation amplifier for resetting the channel counter means at a selected point in the EKG signal.
15. The system as set forth in claim 12 wherein said indication producing means includes a cathode ray display tube operatively connected with said memory, a video time base generator operatively connected to said memory and to said cathode ray tube for generating line SYNC pulses for controlling the sweep of the cathode ray tube and for causing said channels to be addressed incrementally at the same rate as the line SYNC pulses, whereby each channel will be displayed with each SYNC pulse which starts a line sweep deflection signal.
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US4294259A (en) * | 1977-11-25 | 1981-10-13 | Bios Inc. | Method and apparatus for characterizing blood flow through the heart |
US4245646A (en) * | 1978-06-19 | 1981-01-20 | Picker Corporation | Nuclear cardiology apparatus and method |
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CN112258432B (en) * | 2020-10-23 | 2021-09-21 | 成都大学 | Neutron-gamma discrimination method based on composite structural element mathematical morphology |
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US3221731A (en) * | 1962-05-31 | 1965-12-07 | Annis Martin | Apparatus for evaluating the condition of the heart muscle |
FR89229E (en) * | 1965-02-22 | 1967-05-26 | Aquitaine Petrole | Apparatus for measuring the logarithmic decrement of an exponential function and its application to the measurement of blood flow by radioactive tracer |
US3824399A (en) * | 1971-01-27 | 1974-07-16 | Saab Scania Ab | Method of in vivo examination of organ functions |
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- 1976-06-25 JP JP51075397A patent/JPS6052387B2/en not_active Expired
- 1976-10-19 ZA ZA766228A patent/ZA766228B/en unknown
- 1976-10-26 NL NL7611844A patent/NL7611844A/en not_active Application Discontinuation
- 1976-10-26 IL IL50764A patent/IL50764A/en unknown
- 1976-11-05 SU SU762418209A patent/SU708987A3/en active
- 1976-11-05 BE BE172150A patent/BE848072A/en unknown
- 1976-11-05 BR BR7607399A patent/BR7607399A/en unknown
Also Published As
Publication number | Publication date |
---|---|
JPS5259977A (en) | 1977-05-17 |
AU1266176A (en) | 1977-10-13 |
BR7607399A (en) | 1977-09-20 |
IL50764A (en) | 1979-03-12 |
JPS6052387B2 (en) | 1985-11-19 |
BE848072A (en) | 1977-03-01 |
GB1527590A (en) | 1978-10-04 |
DE2617886A1 (en) | 1977-05-12 |
IL50764A0 (en) | 1976-12-31 |
SU708987A3 (en) | 1980-01-05 |
NL7611844A (en) | 1977-05-10 |
AU501106B2 (en) | 1979-06-14 |
ZA766228B (en) | 1977-09-28 |
FR2331038B1 (en) | 1982-10-22 |
FR2331038A1 (en) | 1977-06-03 |
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