The present invention relates to medical diagnostic systems, and more particularly to an integrated electrophysiology and ultrasound imaging catheter system.
Advancements in miniaturization of ultrasound technology has enabled the commercialization of catheters including phased array ultrasound imaging transducers small enough to be positioned within a patient's body via intravenous cannulation. By imaging vessels and organs, including the heart, from the inside, such miniature ultrasound transducers have enabled physicians to obtain diagnostic images available by no other means.
Another important cardiac diagnostic technology is intracardiac electrophysiology recorders, which include catheters with multiple electrodes on a distal end that can be positioned within a patient's heart to record electrical signals passing through heart tissue. Electrophysiology catheters and the associated analyzer equipment provide the clinician with important information regarding root causes of heart arrhythmia, dyssynchrony and other irregular heart beat maladies.
Given the diagnostic advantages of intracardiac ultrasound imaging and electrophysiology analysis, many diagnostic procedures make use of both technologies to better diagnose heart disease. However, the large cart used to hold ultrasound imaging equipment and the large cart used to hold electrophysiology equipment take valuable up space in the catheterization lab. Just as important, the separate ultrasound imaging and electrophysiology systems require the operating clinicians' attention, increasing their workload during the risky catheterization procedure.
The present invention is directed toward providing an integrated electrophysiology and ultrasound imaging system which can provide a single operating interface for these diverse medical diagnostic systems. A single workstation is able to receive and analyze intracardiac electrophysiology signals, such as from intracardiac electrophysiology catheters while controlling and receiving data from an ultrasound imaging catheter system. In an embodiment, a compact, portable ultrasound beamformer unit is connected to and controlled by a workstation that is also configured to perform/control electrophysiology analysis. The portable ultrasound beamformer unit includes a compact, integrated ultrasound pulse generation, beam forming, and electrical isolation unit with connectors for connecting to one or more ultrasound transducer arrays and an image display unit. An ultrasound imaging catheter can may be connected to the ultrasound beamformer unit.
The accompanying drawings, which are incorporated herein and constitute part of this specification, illustrate exemplary embodiments of the invention, and, together with the general description given above and the detailed description given below, serve to explain features of the invention.
Various embodiments of the present invention will be described in detail with reference to the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or like parts.
As used herein, the terms “about” or “approximately” for any numerical values or ranges indicate suitable dimensional tolerances that allow the part or collection of components to function for their intended purposes as described herein. Also, as used herein, the terms “patient”, “host”, and “subject” refer to any human or animal subject and are not intended to limit the systems or methods to human use. Further, embodiments of the invention will be described for use with an intracardiac ultrasound transducer array catheter. However, the embodiments may be applicable to any medical ultrasound transducer.
Common cardiac diagnostic procedures involve positioning electrophysiology catheters near or within a patient's heart in order to obtain and record electrical signals passing through the heart with each heartbeat to assess the heart's health. Frequently an ultrasound imaging catheter will also be positioned with the patient's heart to obtain images of portions of the heart, measure blood flow through the heart chambers and valves and observe the movement of the heart with each heartbeat. These procedures are typically conducted simultaneously in a hospital “cath lab” since they both involve catheterization requiring positioning of catheter tips at precise locations in the heart. Also, cardiologist will consider electrophysiology data in conjunction with cardiac ultrasound data when diagnosing several types of cardiac disease.
Heretofore, the electrophysiology workstation and ultrasound imaging workstation have been separate systems housed in different equipment physically and electrically isolated one from another. The functions and designs of electrophysiology and ultrasound systems are incompatible which, until this invention, have required the separate equipment. In particular, the electrophysiology workstation must sense and record extremely weak voltages that pass through heart tissue and picked up by small electrodes on the electrophysiology electrodes. The electrophysiology workstation must amplify these very weak signals without distortion while filtering out external electrical noise. In contrast, the ultrasound imaging workstation must generate high frequency electrical pulses for each of the ultrasound transducers (typically 64 transducers) within the ultrasound imaging catheter, provide these pulses to the ultrasound imaging catheter, and then receive the high frequency echo signals returning from the transducers. The generation and processing of ultrasound electrical pulses would be a source of electrical noise that would interfere with electrophysiology readings if the two systems were integrated within a single workstation. Solutions to such interference might be possible, but only with expensive and complex electrical and physical isolation measures that would increase the cost of an integrated system beyond the cost of separate systems. Thus, the conflicting design requirements and electrical functions of electrophysiology and ultrasound systems have kept the two systems separated.
As a consequence, clinicians conducting electrophysiology and intracardiac ultrasound imaging examinations must monitor and control two separate systems on separate workstations. This adds to the clinician's workload. Also, the presence of two separate systems take up space in the cath lab which is already crowded with catheterization equipment, fluoroscopy systems and other diagnostic equipment.
The present invention integrates the control and display function for an intracardiac ultrasound imaging system within an electrophysiology analyzer by employing an integrated beamformer and isolation box to provide electrical isolation of ultrasound generation/processing electronics from the electronic filters and amplifiers of the electrophysiology equipment. As used herein, an electrophysiology analyzer (or electrophysiology equipment) refers to a multichannel electrocardiogram (ECG) system suitable for receiving and analyzing electrical signals received by one or more intracardiac electrophysiology catheters. A suitable electrophysiology analyzer for use in the various embodiments is the EP-WorkMate® electrophysiology workstation manufactured by EP MedSystems, Inc. of West Berlin, N.J.
In overview, an embodiment provides an integrated workstation with electrophysiology analyzer processing circuitry that includes communication interfaces and functionality for receiving processed ultrasound data from and providing commands to an integrated ultrasound beamformer and isolation box. Image processing and display capabilities are included in the integrated workstation with the capability of displaying both electrophysiology and ultrasound data and images, as well as combined images. The integrated workstation includes a communication interface for sending command signals to the ultrasound system. Such signals will include the standard ultrasound system commands, but may also include ECG signals which may be used to gate or otherwise control ultrasound imaging. The integrated workstation further includes control interface displays and human interface devices (e.g., keyboard, mouse, light pen, touch screen display, etc.) to enable a user to control both electrophysiology and ultrasound imaging process from a single interface. By the eliminating the need for a separate ultrasound analyzer and display system, the various embodiments reduces the number of separate systems needed within the hospital's cath lab.
In an embodiment, a cable (or multiple cables) provide an electrical connection between the integrated electrophysiology/ultrasound workstation and the beamformer/isolation box. In another embodiment, a wireless data link provides a data communication connection between the integrated electrophysiology/ultrasound workstation and the integrated beamformer/isolation box. Embodiments using wireless data and control links reduces problems with electronic noise of ultrasound pulses leaking into electrophysiology data.
In an embodiment, the system also includes software for generating an ultrasound image display within or adjoining the electrophysiology display. The display may generate a combined ultrasound and electrophysiology display, such as overlaying EP data on ultrasound images, or side-by-side displays.
Main elements of the various embodiments are illustrated in the block diagrams of
For all medical imaging technologies, patient safety is of paramount concern. For imaging technologies involving intrabody probes (e.g., ultrasound imaging catheters, electrophysiology (EP) catheters, ablation catheters, etc.), particular attention is paid to protecting the patient from unintended electrical currents and power emissions within the patient's body. For example, testing has shown that leakage currents of sufficient strength can cause muscle stimulation, which may be detrimental to the patient undergoing intrabody imaging. As such, industry approved electrical safety standards (e.g., for isolation, grounding, and leakage current) have been established for medical devices, such as national standards set by the Association for Advancement of Medical Instrumentation, limiting leakage currents from intracardiac probes to less than 50 microamperes.
In typical catheter based probes, electrical shielding or insulation is provided by way of a robust catheter body to satisfy the industry approved electrical safety standards. Shielding alone, however, may be unsatisfactory for some implementations, as substantial shielding increases the thickness of the catheter body. Induced currents may also arise from the catheters acting as an antenna picking up electromagnetic energy radiated by electronic equipment present in a typical electrophysiology lab. In some instances, the shielding may be inadvertently damaged and, thus, not provide adequate protection. Thus, methods and devices that enable intracardiac medical devices to meet or exceed the federally mandated electrical safety standards are highly desirable.
Published research has revealed that the human heart is more vulnerable to small currents when the currents are introduced within the heart itself, such as by percutaneous catheters. In Cardiovascular Collapse Caused by Electrocariographcally Silent 60 Hz Intracardiac Leakage Current, by C. Swerdlow et. al., the authors reported that leakage currents as low as 20 microamps may induce cardiovascular collapse when applied within the heart. Accordingly, percutaneous catheters might require greater electrical isolation than specified in more general standards in order to assure patient safety.
Such small leakage currents can readily arise, for example, from imperfect electrical insulation, condensation in circuits, faulty electronic components, ambient radio waves, and induction from surrounding circuits and magnetic fields. Further, safety standards require minimum (“creepage”) distances (such as 5 millimeters) between certain conductors to isolate a patient from possible high voltage discharges resulting from unlikely but possible component failures.
For these reasons, both intracardiac electrophysiology and ultrasound imaging catheters must be electrically isolated from the analyzer systems by means of electrical isolation circuitry 44. Heretofore, such electrical isolation has been provided by an isolation box containing isolation circuitry which connects to catheters (both ultrasound and EP catheters) on one side and the analyzer systems on the other.
Isolation circuitry 44 isolates unintended, potentially unsafe electrical currents and voltages from the transducer array 22 which contacts the patient. Examples of suitable isolation circuits are described in U.S. patent application Ser. No. 10/997,898 “Method And Apparatus For Isolating A Catheter Interface”, published as U.S. Patent Publication No. 2005/0124898 to Borovsky et al filed on Nov. 29, 2004, the entire contents of which are hereby incorporated by reference. An example of such safety methods and systems is embodied in the ViewMate® catheter ultrasound system from EP MedSystems, Inc. of West Berlin, N.J.
In various embodiments, the isolation circuitry 44 is integrated with ultrasound beamformer circuitry in an integrated ultrasound beamformer unit 40. For this reason, the system description begins with a description of the details of the ultrasound beamformer unit 40. While the following description address embodiments in which the ultrasound beamformer unit 40 is a separate box, in another embodiment this unit 40 is included on or within a structure housing the electrophysiology analyzer 60 and display unit 70.
The ultrasound beamformer unit 40 may include a housing or chassis with exterior connectors for connecting cables to other elements of the embodiment. The ultrasound beamformer unit 40 may contain optical and electronic circuitry implementing some or all of the elements described in the following paragraphs. The component elements and interconnecting circuitry of ultrasound beamformer unit 40 may include one or more large scale integrated circuits such as VLSI, ASIC, and FPGA chips mounted on one or more circuit boards which are coupled to the connectors.
A signal cable 28 delivers ultrasound signals from ultrasound beamformer unit 40 to each of the transducers in the array 22. Typically, the signal cable 28 will include at least one wire per transducer, and in an embodiment, includes a coaxial cable connected to each transducer in the array 22. In an alternative embodiment, the signal cable 28 includes fewer wires than transducers and a multiplexer circuit (not shown) configured to enable signals to and from the plurality of transducers over the wires. Typically, the signal cable 28 includes an electrical connection plug (e.g., a standard connector) on the proximal end. Providing a plug connector on the end of the cable 28 allows completion of the many electrical connections between the cable conductors and the ultrasound beamformer unit 40 since the connection can be accomplished by pressing the plug into a complementary connector in the housing 100 of the ultrasound beamformer unit 40.
The transducers in the array 22 convert the electrical signals from the ultrasound beamformer unit 40 into sound waves, which propagate into a portion of a patient's anatomy, such as the heart. The same transducer array 22 also receives ultrasound echoes reflected from anatomic structures and transforms the received sound into electrical signals (e.g., by means of the piezoelectric effect). These electrical signals are conducted via cable 28 back to the ultrasound beamformer unit 40.
Signal generator 46 generates electrical signals of ultrasonic frequencies to be provided to the ultrasound transducer array 22. The signal generator 46 can be configured to produce signals of particular wave forms, frequencies and amplitudes as desired for imaging tissue. The signal generator 46 may also be configured to generate signals with the necessary phase lag to enable the transducer array to generate a focused and steerable sound beam as well known in the art of imaging ultrasound phased array transducers. Alternatively, phase lag may be added by another circuit, such as a beam former circuit 54.
A transmit/receive multiplexer circuits 48 can be included to direct the signals generated by the generator 46 to isolation circuitry 44 and to separate out echo signals returned from isolation circuitry 44 from the generated signals.
A thermal monitoring circuit 42 and a cut-off circuit 43 may be included to mitigate possible risks to the patient that can result from excessive local heating by ultrasound. For example, the thermal monitoring circuit 42 may be connected to a temperature sensor (not shown), such as a thermoresistor (“thermistor”) positioned on the catheter near the transducer array 22. The thermal monitoring circuit 42 is preferably configured to determine from signals received from the temperature sensor when temperatures in the vicinity of the transducers exceed a safe threshold value and to trigger a safety action when the threshold is exceeded. The safety action may be the output of a cut-off signal to a cut-off circuit 43 which is configured to shut off the signal generation, disconnect transmit circuits from the transmission cable 28, or otherwise discontinue the transmission of ultrasound pulses to the transducer array 22 in response to a cut-off signal. Examples of suitable temperature sensors, thermal monitor circuits and cut off circuits are provided in U.S. patent application Ser. No. 10/998,039 entitled “Safety Systems And Methods For Ensuring Safe Use Of Intra-Cardiac Ultrasound Catheters” published as U.S. Patent Publication No. 2005/0124899 to Byrd et al. filed on Nov. 29, 2004, the entire contents of which are hereby incorporated by reference.
In an embodiment, the thermal monitor circuit 42 is configured to monitor temperature of the catheter as sensed by a thermistor on the catheter, and to transmit to the display unit 70 a temperature value that may be displayed on a monitor. The thermal monitor circuit 42 in such an embodiment may calculate the catheter temperature value or estimate the intracardiac tissue temperature value and transmit this value as digital data to the display unit 70. The thermal monitor circuit 42 may also be configured to transmit a warning when the measured temperature exceeds a threshold, such as a temperature that is elevated but still safely below a level at which tissue damage may occur. Such a warning would inform clinicians of a potentially hazardous condition to permit them to take actions to reduce heating, such as adjusting ultrasound power or duty cycle parameters, in order to avoid damaging tissue and automatic shutoff by the cut-off circuit 43. Such a warning may be transmitted to the display unit 70 as digital data for display on the monitor (image display unit).
In another embodiment, a display, such as colored light emitting diode (LED) indicators (45G, 45Y, 45R) on the ultrasound beamformer unit 40 are provided to indicate temperature information, in the alternative or in addition to displays on to the display unit 70. For example, in such an embodiment three LEDs may be provided, such as a green LED 45G to indicate a safe detected temperature, a yellow LED 45Y to indicate an elevated but marginally safe temperature, and a red LED 45R to indicate an unsafe or near unsafe temperature. In such an embodiment, the thermal monitor circuit 42 includes circuits configured to light the appropriate colored LED based upon the measured temperature. This configuration may be accomplished by the thermal monitor circuit 42 testing the sensed temperature against two threshold values, wherein the first threshold corresponds to elevated but still safe temperatures and the second threshold corresponds to unsafe or near unsafe temperatures. Thus, the thermal monitor circuit can be configured (e.g., with digital switches) to power (i.e., direct a voltage to) the green light emitting diode in response to the temperature input signal indicating a sensed temperature less than the first threshold, power the yellow light emitting diode in response to the temperature input signal indicating a sensed temperature greater than the first threshold but less that the second threshold, and power the red light emitting diode in response to the temperature input signal indicating a sensed temperature greater than the second threshold.
A filter and conditioner circuit 51 can be included in the ultrasound beamformer unit 40 to reject spurious signals that may be induced in or through cable 28.
An analog-to-digital converter (ADC) 52 can be included in the ultrasound beamformer unit 40 to frequently sample and convert the ultrasound signals from analog electrical levels to discrete digital numeric values.
A signal buffer 53 can be included to store at least a portion of the echo signals, which are returned from the transducer array 22 and which may be processed by other elements of the ultrasound beamformer unit 40. In an embodiment, a signal buffer 53 is included to store the echo signals as digital data in a random-access semiconductor memory (RAM).
Beam former 54 circuits may be included to process signals sent to and received from the transducer array 22 to enable phased-array ultrasound imaging. The beam former 54 may receive ultrasound signals from the signal generator 46 and introduce phase lags for each transducer element so that when the signals are applied to the transducer elements a narrow beam of sound emanates from the array. Also, the beam former 54 may receive signals from the transducer array and process the ultrasound echo signal data to calculate the amplitude and direction of the ultrasound echoes returned to the transducer array 22 from each of many specific angles and distances. The beam former 54 may also determine the frequency or Doppler frequency shift of the signal returned form each of selected angles and distances from the transducer array 22.
A communications transceiver 58 may be included to prepare ultrasound data for transmission out of ultrasound beamformer unit 40, typically in digital form. The communication transceiver 58 may also receive data and commands from outside the ultrasound beamformer unit 40 and convert such signals to a form usable by the ultrasound beamformer unit 40. Data transmission may by any high speed (e.g., gigabit per second) data link, such as Ethernet. In an embodiment, the communications transceiver 58 may also transmit electrophysiology signals to the electrophysiology analyzer 60.
In an embodiment, the communications transceiver 58 may include data encoding or compression capability, such as a microprocessor programmed with data encoding or compression software, so that the ultrasound data can be transmitted in a compressed format. By transmitting data in a compressed format, lower bandwidth communication links (e.g., cable or wireless data link) can be used to transmit data, or more data can be transmitted over a standard cable or wireless data link. Additionally, the control unit 41 or other modules may be configured to filter out data that need not be transmitted, such as signals or data pixels containing little or no data (i.e., pixels where little or no echoes were received), so such data need not be transmitted. In yet a further embodiment, the communications transceiver 58 may include temporary storage capability (e.g., random access memory) and be configured to manage the transmission of data at a maximum data rate consistent with the communication link even when data provided to the transceiver exceeds the maximum data rate. Suitable circuitry and software for encoding, compressing, buffering and filtering data and managing data transmission are well known in the communications arts.
The ultrasound beamformer unit 40 may include a control unit 41 which may be a microcontroller, a microprocessor, a microcomputer, or other controller circuitry (such as programmable firmware or a programmable gate array). The control unit 41 may be configured to coordinate the activity and functionality of the various elements included in the ultrasound beamformer unit 40.
In an embodiment associated with cardiac imaging, the ultrasound beamformer unit 40 may also include electrical connections for receiving signals from electrocardiogram (ECG) electrodes and for passing such signals on to an external electrocardiogram (ECG) unit 60 which may be connected to the ultrasound beamformer unit 40 through a communications interface 62. The communications interface 62 may be any wired or wireless interface. In an embodiment, the ECG electrodes can be an intracardiac ECG catheter 64 which includes one or more electrodes 66 near a distal end for sensing electrical activity in the heart. Electrical signals sensed by the electrodes 66 can be conveyed to the ultrasound beamformer unit 40 by means of an extension of the catheter 64 or a connecting cable 68. In various embodiments, the ECG catheter 64 is connected to the isolation circuitry 44 which isolates the patient from stray or fault voltage from the external ECG equipment 60. In an embodiment, signals sent by the ECG 60 through the interface 62 can be recorded or used to synchronize received ultrasound image data with the heartbeat of the patient. For example, a sequence of images may be associated with a sequence of ECG readings revealing the phases of the cardiac cycle, or images may be captured only at a specified phase of the cardiac cycle.
In an embodiment in which the ultrasound beamformer unit 40 may be packaged within a single housing (see
The relationship, function, and interaction of the elements which may be contained in the ultrasound beamformer unit 40 of an embodiment will be described further with reference to
In the various embodiments, the image display unit 70 may be a computer, such as a laptop or workstation, which can be configured to perform more sophisticated image processing then is provided by the ultrasound beamformer unit 40. Such an embodiment will be described later (with respect to
Optionally, there may be two (or more) separate communication interfaces 75: one interface for the ultrasound image data communicated to the display unit 70, and a second interface (not shown in
In the embodiment illustrated in
In an alternative embodiment, the data interface 75 may be an optical cable, such as one or more fiber optic cables. This embodiment is illustrated in
In some embodiments, the communications transceiver 58 and/or the data interface 75 are configured to recognize the particular type of communication link connected to the ultrasound beamformer unit 40, and to adapt the communication protocols, data encoding and data transmission rates to match the connected link. Such embodiments may also include software programmed in the microcomputer 41 that enables it to supervise the ultrasound beamformer unit 40 consistent with the capabilities and requirements of the connected data link. In such embodiments, the ultrasound beamformer unit 40 may include a number of different connection ports for various communication links, such as two or more of a USB port, a FireWire port, a serial data port, a parallel data port, a telephone band modem and RJ-11 port, a WiFi wireless data link and a BlueTooth wireless data link, for example. Circuitry and/or software operating in the communication modules or microprocessor 41 can be configured to sense when a particular one of the various accommodated communication links is connected, such as by sensing an electrical or radio frequency signal received by the link. Recognizing that a particular link is connected, the communications transceiver 58 and/or the data interface 75 and/or microprocessor 41 can implement the protocol, data encoding and data transmission rate that corresponds to that link. Circuits and methods for recognizing connected data links and adjusting communications protocols accordingly are well known in the digital communication arts. Such embodiments provide flexibility of use, allowing users to connect displays and processors using available or convenient cables or communication links.
Functionality within the ultrasound beamformer unit 40 can be managed and timed by a programmed microcontroller, a microprocessor, a microcomputer 41, equivalent firmware, an ASIC chip, or discrete electronic circuitry, all of which are encompassed by description references to “microcomputer” herein. The microcomputer 41 can respond to configuration parameters and commands sent from the image display unit 70 over communication interface 75. Examples of such configuration parameters and commands include the frequency of the generated ultrasound signals, the mode of operation (continuous or pulsed), depth of imaging, angular width of the active image area, amplifier gain, filter frequencies, details about the transducer array 22 (number and arrangement of transducers), and so forth.
The hardware layout and software programming needed to implement the design and programming of the ultrasound beamformer unit 40 are typical and well known to electrical and software engineers skilled in this art. Similarly, the algorithms programmed into display unit 70 are known to software engineers skilled in mathematics, computer graphics, and graphical-interface operating systems.
The image display unit 70 can perform any number of several functions. The display unit 70 can process and display the electrophysiology data provided by the electrophysiology analyzer 60 and ultrasound image data provided by the ultrasound beamformer unit 40 on a connected monitor 73 or other display, such as a large plasma screen display (not shown) coupled to the display unit 70. The display unit 70 can transmit configuration parameters and control commands to the ultrasound beamformer unit 40, where the configuration parameters and commands may be supplied by the operator of the system by means of interactive inputs from a pointing device (mouse or joystick) and keyboard attached to or part of the display unit 70. For example, the operator may inform the display unit 70 about the type of imaging catheter 20 which the display unit 70 may further translate into operational details about the transducer array 22 included in the imaging catheter 20.
In some embodiments, a portion or all of the electrophysiology analyzer 60 functionality is integrated within the display unit 70. A typical electrophysiology system receives electrical signals from electrophysiology catheters 64, amplifies and digitizes the signals, displays the EP signals on a display 73, and stores the EP signals and electrocardiograms for off-line analysis. The electrophysiology analyzer 60 may record a large number of channels of data, such as up to 192 channels, as each electrophysiology catheter 64 may have a large number of electrode sensors 66 and multiple (e.g., two or three) electrophysiology catheter 64 may be used simultaneous. The electrophysiology system may also incorporate an integrated stimulator for providing electrical stimulation to the heart, and an interface for an ablation system for ablating heart tissue using an ablation catheter. The electrophysiology analyzer 60 may provide the clinician with a number of analysis tools and functions for viewing the EP waveforms and analyzing the data for diagnostically meaningful information. For example, the electrophysiology analyzer 60 may determine timing intervals between different ECG wave components (e.g., R-R, A-A, A-H, H-V, V-V, V-A), displayed both as waveforms and as numerical values. The analysis and display of EP data may be in real time or historical, or both such as to compare current measurements with baseline or pre-treatment measurements. Additionally, the electrophysiology analyzer 60 may provide additional functionality depending upon the processor's software, such as: activation mapping; Holter window; pace mapping tools; ablation system control and settings window; cine capture; post acquisition processing; stimulator system control window; database management with query capability; data exporting/communication capability (e.g., faxing capabilities); and other signal analysis tools. Many of these electrophysiology system functions can be performed by the processor associated with the display unit 70. Thus, as illustrated in
Similarly, some of the functionality described herein as residing within the ultrasound beamformer unit 40 may be provided within the display unit 70 as software provided functionality of the processor. For example, in some embodiments, the image display unit 70 processor can convert the ultrasound data generated by the beam-former 54 (which may be relative to a transducer-centered polar coordinate system) into an image relative to another set of coordinates, such as a rectangular coordinate system. Such processing may not be necessary in the display unit 70, if the conversion was already preformed in the ultrasound beamformer unit 40. Techniques for converting image data from one coordinate system into another are well-known in the field of mathematics and computer graphics.
The display unit 70 may display the electrophysiology data and ultrasound image data as an image on a standard video monitor 73 or within one or more graphics windows managed by the operating system (such as Microsoft Windows XP) of the display unit 70. In addition, the display unit 70 can display textual data for the operator on the monitor 73, including, for example, information about the patient, the configuration parameter values in use by the ultrasound beamformer unit 40, and so forth. In an embodiment, the display unit 70 may provide a function that allows measuring the distance between two points on the image, as interactively selected by the operator. Additionally, the display unit 70 may provide various electrophysiology data analysis tools as described above. Examples of integrated electrophysiology and ultrasound image displays are provided in
To analyze and display an indication of motion—and specifically the velocity of movement—of locations in the image corresponding to tissue and fluid movement (i.e., blood), further Doppler frequency distribution analysis can be performed and translated into a readily understandable graphical representations. Doppler frequency analysis is well-known in the field of ultrasound medical imaging and described in more detail in the patent applications incorporated by reference herein. Fourier analysis may be used, for example, to determine the frequency distribution information and the average Doppler frequency shift for each of all points or selected points in the ultrasound image, and from which to compute the individual velocities of those points.
The display unit 70 can generate an image in which the Doppler frequency shift information communicated by the ultrasound beamformer unit 40 for each point or pixel is represented by a color hue. Since Doppler shift provides information on the speed and direction of movement of fluids and structures with respect to the transducer, various color hues can used in the display to correspond to the velocity and direction of motion. For example, red may be used to represent the maximum velocity in one direction, blue to represent the maximum velocity in the opposite direction, and colors between red and blue on the color spectrum to represent velocities in between. In another embodiment, such colors can be superimposed on the B-mode image, which is otherwise rendered as a gray-scale image wherein the brightness of each pixel depends on the amplitude of the returned ultrasound echo from the anatomical location corresponding to the pixel. Other modes of display are well known in the art, such as a plot of the distribution of Doppler frequency shifts at the points along a line in the image, and M-mode in which the movement along narrow lines is displayed.
Optionally, a connection interface 92 may connect the display unit 70 to a clinic or hospital information infrastructure 90 or the Internet. A hospital information infrastructure 90 will typically include a network of attached workstations, graphical displays, database and file servers, and the like. The optional interface 92 typically can be an Ethernet cable, a wireless WiFi interface (IEEE 802.11), or any other high-speed communications physical layer and protocol. For example, an interface 92 can allow the display unit 70 to access information from the Internet, a database, or a hospital network infrastructure 90. The display unit 70 may also transmit information outward via the interface 92, such as to store the ultrasound data on a network server or display the ultrasound images elsewhere than the display unit 70.
Physically isolating the ultrasound beamformer unit 40 from the electrophysiology analyzer 60 and display unit 70 also prevents high frequency noise from the ultrasound pulses, such as created by the ultrasound signal generator 46, from interfering with the reception, amplification and analysis of electrophysiology signals received by the electrophysiology catheter 64. As noted above, such relatively high power, high frequency pulses could overwhelm the electrophysiology signals if not properly shielded from the electrophysiology analyzer 60. A wireless data link 76, as shown in
In the embodiment illustrated in
Commercially available wireless communications systems can be used for the wireless interface 76. For example, the wireless interface 76 may be an infrared communication interface (such as the IRDA standard), a radio-based communication interface (such as the Bluetooth, ZigBee, or 802.11 WiFi or 802.15.4 standards), or both (for example, infrared in one direction and radio in the other direction). To decrease the data processing that must be done in the ultrasound beamformer unit 40, a high speed data transmission system may be used to provide partially processed ultrasound data to the image display unit 70 for further processing. The data transmission may have a data rate of 1 megabit per second or more.
Common to the embodiments illustrated in
A self-contained power source, such as a battery or solar cell, can provide inherent safety advantages over conventional power sources. This is because a self-contained power source 59 can be used to further isolate the patient from stray and fault currents since there need not be a power cable connected to the beam former unit. This removes the power source (such as hospital main AC power) and the power cord as sources of power spikes and fault currents. Such isolation may be further enhanced by forming the housing or chassis of the ultrasound beamformer unit 40 from non-conductive material and encasing the self-contained power source within the housing or chassis. This configuration effectively presents no return path or common ground between the power source and the patient. That is, even if there is an electrical potential difference between the ultrasound beamformer unit 40 and the patient, little current can flow between them. Further, with a self-contained power source, there is very little chance that a patient will receive high voltage from lightening or from a utility power outlet through a failed component, faulty design, or a power surge. A typical self-contained power supply 59 can supply only limited current at limited voltage, further reducing the likelihood of excessive leakage current. Also, using a self-contained power supply 59 can further reduce cables and conductors which can pick up stray electromagnetic radiation and become a source of electronic noise in the system.
In another embodiment, the power supply 59 may be power conductors parallel to or contained in the communication cable 75 of
If an embodiment does use an electrically conductive cable as part of the communication interface 75, then in lieu of other measures, the data communication interface 75 can include additional circuits for isolating the ultrasound beamformer unit 40 from any source of excessive leakage current or high voltage from or through the display unit 70—whether or not power is supplied over the interface 75. National and international safety organizations specify leakage current and breakdown voltage standards for various medical applications: for example, a maximum leakage current of 20 microamperes or a breakdown voltage of at least 5000 volts. By providing electrical isolation circuitry 44 within the ultrasound beamformer unit 40, greater protection for the patient can be provided against high power, power surges, and system overloads, as well as providing greater protection against or filtering of signal artifacts, signal jitter, and signal crosstalk.
Further patient electrical isolation is provided in embodiments utilizing a fiber optic data cable 75 between the ultrasound beamformer unit 40 and the display unit 70. In an alternative embodiment, further isolation may be provided by including an optical isolator module somewhere along each conductor of the interface 75. An example of an optical isolator module includes a light-emitting diode optically coupled to a photo detector and configured so that electrical signals entering the module are converted into light signals and converted back into electrical signals within the module, thereby conveying the data across an electrically isolating space. In embodiments where the data interface 75 is an optical fiber with suitable optical-electrical converters at each end of the interface 75, the optical fiber cable can be constructed to prevent or minimize electrical conduction, such as fabricating the covering from non-conducting plastics, thereby providing better electrical isolation. Optical isolation may preclude supplying electrical power through the data interface 75, so an alternative power supply 59 for the ultrasound beamformer unit 40 according to an embodiment described herein may be employed. The use of optical fiber cable or an optical isolation can also help to reduce electronic noise introduced into the ultrasound beamformer unit 40 from stray electromagnetic radiation.
In the various embodiments, the ultrasound beamformer unit 40 lies between the patient on one side and power sources and external processors/displays on the other. As such, different levels of isolation may be provided by separate isolation circuitry 44 within the ultrasound beamformer unit 40 as appropriate to particular connections. For example, by providing greater electrical isolation on connections to power and/or external processor/displays, such isolation may protect the circuitry of the ultrasound beamformer unit 40 as well as the patient from external voltage spikes and fault currents. As another example, isolation circuitry on the patient side of the ultrasound beamformer unit 40 circuitry, may reduce hardware and software complications and increase integration efficiency.
Simultaneously positioning an ultrasonic imaging catheter 20 in the heart 12 as shown in
There is a safety concern for intrabody ultrasound systems wherein the ultrasound power may locally heat tissue above a safe body temperature, particularly for the higher power employed by color Doppler imaging. Although the ultrasound generation electronics may indirectly limit the amount of heat an ultrasonic catheter can theoretically induce in tissue at a given power level, direct monitoring of the actual temperature at the transducer array and surrounding tissue is much safer and avoids assumptions about how effectively specific tissues can dissipate the heat. Therefore, a need exists for a safety means either to warn the operator or to curtail the applied power automatically, whenever the measured temperature exceeds some pre-determined limit. An example of a standard safe temperature limit, as established by FDA in the United States, is 43 degrees Celsius, although the exact limit may depend on the specific environment and use of the catheter.
To address this safety concern, the catheter 20 may optionally further include an electronic temperature sensor 26, such as a thermocouple or thermistor, as shown in
Examples of phased array ultrasound imaging catheters used in performing intracardiac echocardiography and methods of using such devices in cardiac diagnosis are disclosed in the following published U.S. patent applications—each of which is incorporated herein by reference in their entirety.
2004/0127798 to Dala-Krishna et al.;
2005/0228290 to Borovsky et al.; and
2005/0245822 to Dala-Krishna et al.
It should be noted that the present invention is not limited to the specific ultrasonic imaging catheter assembly disclosed in the applications cited above, because the invention is applicable to various catheters and instruments designed for intravascular and intracardiac echocardiography and for other physiological uses involving an ultrasound beam former and interfaces with medical instruments and external display equipment.
Electrodes 66a-66j, 67a-67g may be spaced approximately 2 mm apart from each other on the catheter 64, with each electrode extending approximately 2 mm in length. Electrodes are preferably made of stainless steel, platinum, gold or other electrode material, and may be formed as thin flexible films applied to the exterior of the catheter body. The electrode array may extend over a length of approximately 35-40 mm of the catheter 64. Electrical wires (not shown) from each electrode are positioned within and pass through the interior of the catheter 64 to a manifold 122 secured to the proximal end 116 of the catheter 64. Each electrode can be coupled to its own connector 124 that can be connected to the electrophysiology equipment 60.
As illustrated in
An example of an electrophysiology catheter is the One-Piece™ Electrophysiology Catheter, part number EPC-E65P252, manufactured by EP MedSystems, Inc. of West Berlin, N.J.
Another example embodiment of the thermal monitor circuit 42 includes a plurality of gate circuits configured to gate the individual leads passing signals to and from each of the transducer elements in the transducer array 22. So long as the temperature measured by the thermistor 26 remains below a safe level (e.g., not more than 43° C.), the gate circuits remain enabled allowing signals to pass to/from the transducer elements. However, should the temperature measured by the thermistor 26 reach or exceed an unsafe level, the thermal monitoring circuit 42 disables the gate circuits, automatically shutting off the transducer array 22. In another example embodiment, the thermal monitor circuit 42 is configured to disable transmission of ultrasound signals from the ultrasound beamformer unit 40 by disabling the transmit circuitry by signaling the signal generator 46 through a trigger mechanism, such as a hardware interrupt signal. Other thermal monitor circuit embodiments include circuits that disable an array of multiplexers or transmit channel amplifiers that may be used in the ultrasound beamformer unit 40 for generating, controlling, distributing, conditioning and/or transmitting ultrasound pulses to the transducer array 22. The various example embodiments of the thermal monitor and cut-off circuits 42, 43, as well as other suitable circuits, perform the safety function of discontinuing transmission of ultrasound signals from the signal generator 46 through the isolation circuit 44 upon receiving a cut-off signal or sensing an unsafe temperature in the vicinity of the transducer array 22.
The signal generator 46 generates electrical signals of ultrasonic frequencies, such as in the range of about 1 megahertz to 10 megahertz, as are commonly used for ultrasound imaging. The signals may be continuous or may be intermittent pulses. The electrical signals may pass through a transmit/receive multiplexer 48, isolation circuits 44, and a cable 28 to reach the transducer array 22. The electrical signals which reach the transducer array 22 cause the transducers to produce ultrasound signals in the same frequency range generated by the generator 46.
The transmit/receive multiplexer 48 directs the signals generated by the generator 46 through the isolation circuitry 44, which serves to limit unwanted electrical currents and voltages passing into the cable 28.
Signals which transit the isolation circuitry 44 pass into the signal cable 28 which delivers the signals to each of the transducers in the array 22. The cable 28 may include at least one wire per transducer in the array. The transducers in the array 22 convert the electrical signals into sound waves, which propagate into a portion of a patient's anatomy, such as the heart. As shown in
An embodiment of the isolation circuitry 44 is described above with respect to
Multiplexer 48 may be necessary where the generated signals from the generator 46 and the received echo signals both pass through the same isolation circuitry 44 and the same wires of cable 28. Specifically, the transmit/receive multiplexer 48 may be used to separate out the received echo signals from the generated electrical signals from the generator 46. This may be accomplished by connecting the transducer array to the receiving amplifier circuits between generated ultrasound pulses, so the only signals allowed to pass are the received ultrasound echo signals. Alternatively, the electrical pulses of the transmitted pulses may be subtracted from all signals received from the isolation circuitry to yield the received ultrasound echo signals. The multiplexer 48 can direct the received ultrasound echo signals to conditioning circuitry 51 to filter and condition the signals as necessary. The signal can also be amplified, such as within the multiplexer 48, within the conditioning circuitry 51, or by a separate amplifier. At some point, the amplified and filtered echo signal can be digitized by an analog-to-digital converter (ADC) and can be temporarily stored in a signal memory buffer 53, such as random access semiconductor memory (RAM).
For an embodiment which employs separate transducers and conductors for the generated signals and for the received echo signals, separate transformers or mono-directional optical isolators may be used in the isolation circuitry 44. In such an embodiment, the transmit/receive multiplexer 48 may not be included.
The filter and conditioning circuitry 51 may be provided to reject signal frequencies outside a certain range, such as rejecting spurious signals induced in the cable 28, for example. The echo signals may be amplified as part of this circuitry (before, during, and/or after filtering), as part of the transmit/receive multiplexer 48 or elsewhere in the ultrasound beamformer unit 40. Other signal processing may be performed to enhance the desirable properties of the signal returned from the transducer array 22. For example, the signal conditioning circuitry 51 may reject the spurious signals from internal reflections within the catheter.
The analog-to-digital converter (ADC) 52 can be included to frequently sample the received ultrasound signals, which are received as analog electrical levels, and convert them to discrete digital numeric values. This conversion may be performed before, during, or following the action of the filter and conditioning circuitry 51. The signal may be in either analog or digital form or both during parts of the amplification, filtering, conditioning, and storage of the signal. In other words, the filter and conditioning circuitry 51 may apply well-known analog filtering techniques to the signals before digitization, may apply well-known digital filtering methods to the digitized signals, or do both. Techniques for such digital and analog signal processing are well known. There may be an ADC per transducer, or fewer ADCs may used with each being time-multiplexed among multiple transducers. Conversion of signals to streams of digital numbers is a convenience based on the current availability and economy of digital processing, but suitable analog circuits can be used in part or all of the ultrasound beamformer unit 40.
Because contemporary electronics routinely store signals in digital form, the embodiment of
The beam-former 54 processes the returned echo signal data, some or all of which may be stored in memory 53. The beam-former 54 may calculate the amplitude of the ultrasound echo at each of many specific angles and distances from the transducer array. Techniques for beam-forming (either for transmission or for reception) are well known in the fields of ultrasound imaging and in phased array sonar and radar.
The result of the processing of the data stored in buffer memory 53 by the beam-former 54 typically can be a pixel-based image relative to a polar-coordinate system. The beam-former 54 may be implemented in very large scale integrated (VLSI) semiconductor circuits. The beam-former 54 may employ substantial parallel processing of the ultrasound signals from the transducers of array 22. For example, there may be simultaneous computations of more than one beam angle and/or more than one distance along a beam angle.
The amplitude, phase and time of arrival of reflected ultrasound pulses at each transducer in the array 22 can be used by the beam-former 54 to calculate the angle (with respect to the long axis of the transducer array 22) and distance from the array to each echo source. The distance and angle data may then be combined with amplitude (i.e., power of the received echo) to produce (e.g., by processing the data according to an algorithm) a pixel of image data. Alternatively, the beam-former 54 may store or output the processed received ultrasound as data sets comprising data groups of angle, distance and amplitude. In this and like manner, the beam-former 54 can turn the large volume of streaming ultrasound signals into a smaller set of data easily passed over a serial data link 75 for processing or display by a display unit 70. In an embodiment, the beam-former 54 is included in a VLSI chip within the ultrasound beamformer unit 40.
The beam former 54 may compare the frequency of the generated signals with the frequency spectrum of the returned echo signals. The difference in frequency relates directly to the velocity of tissue or blood toward (higher frequency) or away from (lower frequency) the transducer array due to the Doppler effect. The difference in frequency, i.e., the amount of Doppler frequency shift, is indicative of motion of the tissue (including blood) from which the ultrasound reflected. The frequency shift may be determined by mixing the generated signal and received echo signal and detecting the difference frequency. The conversion of the frequency shift to velocity depends on the speed of sound in the body, which is about 1450 to 1600 meters per second in soft tissue, including blood. The conversion of frequency shift to velocity according to well known algorithms may be performed immediately by the beam former 54, or later, such as by an external image processor at the time the image is displayed. If calculated by the beam-former 54, the velocity data (or Doppler shift) may be outputted as a fourth element of the data set, so that echo sources are identified by angle, distance, amplitude and velocity (or frequency or Doppler shift).
The velocity of echo sources may be computed at each of numerous angles and distances relative to the transducer array 22. The computed velocities may be represented visually as a spectrum of colors, for example, as is conventional in the art. The velocity of numerous points in the tissue or blood may be mapped to colors at the corresponding locations in the final image of the tissue. Image display unit 70, as shown in
With reference to
As also shown in
A programmed microcontroller, microprocessor, or microcomputer 41 or functionally equivalent discrete electronics can be included to coordinate the activity described above within the ultrasound beamformer unit 40. In addition, the microcomputer 41 (or equivalent) may respond to configuration parameters and commands sent from the image display unit 70 (of
In an embodiment, the ultrasound beamformer unit 40 may be configured via software or discrete circuits to adaptively cut and separate each frame of ultrasound image data. Such capability may be used to select and transmit frames for which there is useful information (e.g., changes in position of structures) to limit the bandwidth required for transmitting ultrasound images to external displays. In a normal cardiac cycle, portions of the heart are at rest for significant fractions of the cardiac cycle, so numerous images during such intra-contraction periods will contain the same image information. By not transmitting images in which there has been no change since the previous image, the same clinical information may be transmitted at substantially lower data rates. Such processing of image frames may be accomplished by a segmentation module (not shown).
In an embodiment associated with cardiac imaging, an external electrocardiogram (ECG) unit 60 (see
Referring to
In an embodiment, signals from the electrophysiology catheter 64 may be used in lieu of, or in addition to, signals from the electrophysiology analyzer 60. The electrophysiology catheter 64 sensor signals can be used to record or control the timing of the ultrasound image acquisition relative to the cardiac cycle instead of or in conjunction with signals from the electrophysiology analyzer 60. The signals from an electrophysiology catheter 64 may be included within the data stream outputted by the ultrasound beamformer unit 40.
Whether an ECG signal is acquired from an external Electrophysiology analyzer 60 or an attached ECG sensor 66, the interface 60, 68 or cable 28, respectively, may be electrically isolated from the ultrasound beamformer unit 40 to enhance patient safety and reduce electronic noise in the system. For wired interfaces, the isolation may be accomplished by a transformer isolation circuit 44 or an optical isolator as described herein. Protection against electrical leakage currents and high voltage discharges may be accomplished in an embodiment by using a wireless interface for the ECG interface 62.
In addition to including connectors for receiving the input/output connection plugs for ultrasound catheters and ECG sensors or equipment, some embodiments of the ultrasound beamformer unit 40 include connections for additional sensors, such as intracardiac percutaneous leads, subcutaneous leads, reference leads and other electrical leads that may be employed during a procedure. As with ultrasound and ECG connections, such additional lead connections can be coupled to isolation circuitry 44 to provide patient protection. By providing such connections with integrated isolation circuitry, the ultrasound beamformer unit 40 can serve as a central interface unit for connecting all sensors employed in a procedure.
Some or all of the electronic circuitry of ultrasound beamformer unit 40 may be implemented within one or more large scale integrated circuits such as VLSI, ASIC, or FPGA semiconductor chips, as are well known in the electronics art. The program instructions running in the microcomputer 41 may be stored in some form of random access memory (RAM) or read-only memory (ROM) as software or firmware.
Portable ultrasound units, which contain compact signal generation and beam-forming circuitry and which are separate from the display unit 70, are available commercially from Terason, a division of Teratech Corporation (Burlington, Mass.). Some of the details of these portable ultrasound units are described along with associated methods in the following published patent applications—each of which is incorporated herein by reference in its entirety:
2005/0228276 to He et al;
2005/0018540 to Gilbert et al; and
2003/0100833 to He et al.
As shown in
Image data from the scan conversion (and Doppler processing, if any) may be processed by an image renderer 83, formatted, and displayed as an image on a video monitor 73. For example, the rendering circuit 83 may generate a gray-scale image (such as a B-mode image) in which the brightness of each pixel is representative of the amplitude of the ultrasound echo from the anatomical point to which the pixel corresponds.
Besides responding to operator input of configuration information, the interactive control 80 may also respond to operator input controlling how the image is converted, processed, and rendered on the display 73.
The image display unit 70 may perform other functions. For example, the interactive control 80 in the image display unit 70 may transmit configuration parameters and control commands to the ultrasound beamformer unit 40, where the configuration parameters and commands may be supplied by the operator by means of interactive inputs from a pointing device (mouse, trackball, finger pad, or joystick, for example) and a keypad or keyboard 72 attached to display unit 70.
Optionally, the interactive control 80 of the image display unit 70 may forward the image and/or raw data to a network file or database server, to the Internet, to display screen, or to a workstation through a communication interface 92.
In an embodiment, the image display unit 70 circuitry may be included within the ultrasound beamformer unit 40 housing or chassis. This may be accomplished by simply including the image display unit 70 circuitry as another board or VLSI chip within the ultrasound beamformer unit 40. Alternatively, the circuitry and functionality of the components of the image display unit 70 may be incorporated in a VLSI chip that also encompasses the beam-former 54 and/or microcomputer 41 within the ultrasound beamformer unit 40. In such an embodiment, the ultrasound beamformer unit 40 outputs image data as a video signal (e.g., VGA, composite video, conventional television or high-definition video) that can be carried by a cable 75 directly to a display 73 to yield an image on the screen without further processing. In a further embodiment, the ultrasound beamformer unit 40 may output image data as a network compatible signal, such as Ethernet or WiFi, that can be directly coupled to a network.
In the embodiment illustrated in
A user input device 72 may connected to the ultrasound beamformer unit 40 to permit a user to provide commands and operating parameters, such as by way of a keyboard, keypad and/or a user pointing device such as a mouse, touch screen, trackball, light pen, or finger pad. The user input device 72 may include a voice recognition device in lieu of or in addition to a keyboard. The input device 72 may be connected to the ultrasound beamformer unit 40 by a cable, an infrared link, a radio link (such as Bluetooth), or the equivalent, each of which are commercially available.
A display monitor 73 may not be present as part of ultrasound beamformer unit 40. Any of many choices, sizes, and styles of a display 73 may be connected to ultrasound beamformer unit 40. For example, the external display monitor 73 may be a cathode ray tube, a liquid crystal display, a plasma display screen, “heads up” video goggles, a video projector, or any other graphical display device that may become available. The display monitor 73 may be large and may be located conveniently out of the way, such as a plasma screen hung from the ceiling or on a wall. The display monitor 73 may be positioned for better viewing by the physician. There may be more than one display 73, and a display may be positioned remotely, such as in another room or in a distant facility. The display 73 may be connected to the ultrasound beamformer unit 40 by a cable, an infrared link, a radio link (such as Bluetooth), or any equivalent wireless technology.
In an embodiment, the display monitor 73 and/or the user input device 72 may be embodied by a computer terminal, workstation, or personal computer such as a laptop computer. Such an embodiment can be configured to display the graphical output from the image rendering circuits 83 and to pass user inputs on to the interactive control 80 of the ultrasound beamformer unit 40. Alternatively, in an embodiment in which the display monitor 73 and user input device 72 are provided by a computer system, the computer system may operate software enabling it to perform additional image processing on the data received from the ultrasound beamformer unit 40.
The ultrasound beamformer unit 40 may need to be powered by an external power source 59, as was previously discussed with respect to
Because of the priority of safety for a patient, a wired connection between the ultrasound beamformer unit 40 and the user input device 72 may need isolation circuitry to prevent potentially harmful leakage current from flowing from the input device 72 through the ultrasound beamformer unit 40 to the patient. This isolation may be provided by the isolation circuits 44 within the ultrasound beamformer unit 40 shown in
One way to achieve isolation for the input device 72 or display device 73 is to employ a wireless communication link between device 72 and unit 40 and between device 73 and unit 40. Any wireless communication link of sufficient bandwidth, such as those mentioned previously, may be used in this capacity.
The embodiment illustrated by
As illustrated in
Referring to
Additionally, one or more ECG sensor electrical connectors 104 may be provided in the housing 100 to permit electrically connecting ECG sensor connectors 68 to the ultrasound beamformer unit 40 without compromising the environmental seal of the housing 100. On the inside of the housing 100, the ECG sensor electrical connectors 104 may be electrically coupled to the isolation circuit 44 or passed through to an external Electrophysiology analyzer 60 via an ECG unit connector 105. In an embodiment, the housing 100 includes sixty-four or more contact edge connector type ports 105 for connecting sixty-four individual ECG probe elements.
Similarly, a power connector 106 may be provided in the housing 100 for accepting a connector to an external power source 59. Alternatively or in addition, an internal power source, such as an optional battery 110 can be included in the housing 100. Additionally, an output connector 107 may be provided for connecting to an external computer or display unit 73. For example, the output connector 107 may be a video connector (e.g., CGI, VGA or composite video) or a standard two-direction serial connector such as USB, FireWire or fiber optic connector. Similarly, an input connector 108 may be provided in the housing 100 to connect to user interface devices, such as a keyboard or computer 72. Likewise, a network cable connector 109 may be provided for directly connecting the ultrasound beamformer unit 40 to a network.
Full system implementations of various embodiments are illustrated in
Functionality provided in software instructions stored on computer readable memory and implemented on the workstation 69 processor include: receiving, storing and analyzing electrophysiology signals received from an electrophysiology catheter; generating displays of electrophysiology data for presentation on a display 73; generating menu screens for presentation on a display 73 to control electrophysiology data analysis, storage and display; receiving and processing user input in response to electrophysiology menu screens; generating menu screens for presentation on a display 73 to control ultrasound image equipment (including control of the beamformer unit 40); generating menu screens for presentation on a display 73 to control ultrasound image signal data analysis, storage and display; receiving and processing user input in response to ultrasound imaging and analysis menu screens; generating and transmitting control commands to the ultrasound beamformer unit 40 to control operation of the ultrasound imaging equipment; receiving, storing and analyzing ultrasound image data received from the ultrasound beamformer unit 40; generating displays of ultrasound image data for presentation on a display 73; and generating combined displays of electrophysiology data and ultrasound images for presentation on a display 73. The software instructions may further enable the workstation 69 to receive, process and display images and data from other sensors, including for example, X-ray images, such as X-ray images of the heart that can image the catheters at the same time that electrophysiology and ultrasound image data is obtained. The software instructions implemented on the workstation 69 configure the workstation 69 to provide commands to the ultrasound beamformer unit 40 that may include but not be limited to:
Record image;
Freeze image;
Switch modes;
Capture;
Brightness;
Contrast;
Ultrasound Power;
Frequency;
Pulse repetition rate (PRF);
Color area (for color Doppler mode);
Scale;
Focus zone; and
Scan angle.
The software instructions also configure the workstation 69 to receive data and status signals from the ultrasound beamformer unit 40. These data signals and configuration data may include but not be limited to: radiofrequency signals (echo data information); vector processing; scan conversion; and display.
Integrating the ultrasound system control and processing with the electrophysiology system also enables the ultrasound control and data recording to be coordinated with ablation therapies which are controlled by some electrophysiology systems. In an ablation operation, high power radiofrequency energy is applied to tissue through an electrode on a catheter in order to kill a region of heart tissue. Some electrophysiology catheters include one or more ablation electrodes so the same catheter can be used to receive electrophysiology signals and conduct ablation. When ablation RF power is applied, the resulting signal can overwhelm the electrophysiology system, so normally, electrophysiology recording is halted during the time when ablation is applied to the heart. However, ultrasound imaging (and recording of ultrasound images) can proceed during ablation. Thus, an integrated ultrasound/electrophysiology system can control and coordinate ultrasound imaging to ablation therapy, such as by recording ultrasound images during ablation, as well as to electrophysiology monitoring.
An advantage of the embodiments described above is the ability to gather, correlate and co-display electrophysiology data and intracardiac ultrasound images simultaneously.
The various embodiments may be used according to the following method which is illustrated in
An ultrasound beamformer unit 40, such as shown in
The ultrasound beamformer unit 40 then connected to the combined workstation 69, step 152. The workstation 69 is connected to a display monitor 73 may be supplied and connected to the ultrasound beamformer unit 40. A data interface 92 may also be established between the workstation 69 and a clinic or hospital infrastructure 90.
A sterile ultrasound transducer cable 28 is connected between the ultrasound beamformer unit 40 and an ultrasound imaging catheter 20, step 153. The ultrasound catheter 20 is introduced into the patient's body, such as by percutaneous cannulation, and positioned so the transducer array 28 is at a desired location and orientation, such as guided by use of fluoroscopy, step 154. The transducer array 28 may be dynamically repositioned to other locations and orientations.
One or more sterile electrophysiology catheters 64 is introduced into the patient's body, such as by percutaneous cannulation, and positioned so the electrodes are at desired locations in the heart, step 155. Positioning of the electrophysiology catheters 64 may be facilitated with fluoroscopy and/or ultrasound imaging using the ultrasound imaging catheter 20. Once positioned in the desired location, the electrophysiology catheters 64 are connected to isolation circuits in the ultrasound beamformer unit 40 or separate isolation box.
Using menu screens presented on the integrated workstation 69 and user input devices 72, a clinician can initialize and configure the ultrasound beamformer unit 40, step 156. The configuration step may include setting of operational parameters of the ultrasound beamformer unit 40, such as ultrasound frequency, mode of operation, mode of image processing, characteristics of the transducer array 22, anatomical position of the array 22, details about the patient, and so forth. The operating parameters may be changed during operation of the invention. For example, the frequency may be changed to increase or decrease the depth of penetration of the ultrasound energy. As another example, the mode of display may be changed from B-mode (which may help the operator position the array 22 with respect to anatomy) to Doppler mode (e.g., color Doppler) to observe and measure the velocity of motion of blood.
Using menu screens presented on the integrated workstation 69 and user input devices 72, a clinician can initialize and configure the electrophysiology analyzer 60 portion of the workstation 69 to receive, record and display electrophysiology signals received from the electrophysiology catheter(s) 64, step 157.
Once configured, the clinician may then record and display electrophysiology data and ultrasound images, step 158. Data may be stored on hard disc storage and/or transmitted to other locations, such as over the internet. The clinician can review the data on displays and, based on the data obtained, make adjustments to the location of catheters and/or settings of the electrophysiology analyzer 60 or ultrasound beamformer unit 40 settings, step 159.
An embodiment includes some or all of the components described herein as a packaged kit with previously sterilized contents. The contents may include, by way of non-limiting example, a catheter 20 bearing an ultrasound transducer array 22, one or more sterile cables, a sterile enclosure for the ultrasound beamformer unit 40, a battery for the ultrasound beamformer unit 40 (if it is battery powered), and instructions. The kit may further include a cable to connect the ultrasound transducer array 22 to the ultrasound beamformer unit 40. The kit may include a cable to connect the ultrasound beamformer unit 40 to the display unit 70, unless the connection between them is wireless. In lieu of just a sterile enclosure for ultrasound beamformer unit 40, an embodiment of the kit may contain the ultrasound beamformer unit 40 which has been previously sterilized. Any appropriate method may be used to sterilize the contents, such as gamma radiation, which is typically used to sterilize packaged kits in bulk. Some or all of the contents may be disposable or may be sterilizable for reuse.
While the present invention has been disclosed with reference to certain exemplary embodiments, numerous modifications, alterations, and changes to the described embodiments are possible without departing from the sphere and scope of the present invention, as defined in the appended claims. Accordingly, it is intended that the present invention not be limited to the described embodiments, but that it have the full scope defined by the language of the following claims, and equivalents thereof.
The present application is a continuation in part of and claims the benefit of priority to U.S. patent application Ser. No. 11/610,778 entitled “Integrated Beam Former and Isolation for an Ultrasound Probe” filed Dec. 14, 2006, the entire contents of which are incorporated herein by reference.
Number | Date | Country | |
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Parent | 11610778 | Dec 2006 | US |
Child | 11772167 | US |