GUIDEWIRE ULTRASOUND (US) PROBE FOR A MINIMALLY PERTURBING MEASUREMENT OF BLOOD FLOW IN BRAIN VESSEL
20210177376 · 2021-06-17
Inventors
Cpc classification
A61B8/12
HUMAN NECESSITIES
A61B8/5223
HUMAN NECESSITIES
A61M2025/09175
HUMAN NECESSITIES
A61B5/065
HUMAN NECESSITIES
A61B8/4263
HUMAN NECESSITIES
International classification
A61B8/12
HUMAN NECESSITIES
A61B8/00
HUMAN NECESSITIES
Abstract
A medical probe includes a guidewire, a magnetic position sensor, and an ultrasound (US) transducer. The guidewire is configured for insertion into a blood vessel of a patient. The magnetic position sensor is fitted at a distal end of the guidewire and is configured to produce signals indicative of a position of the distal end. The US transducer is fitted at the distal end of the guidewire and is configured to transmit US waves inside the blood vessel, and acquire respective US echoes indicative of blood velocity in the blood vessel.
Claims
1. A medical probe, comprising: a guidewire for insertion into a blood vessel of a patient; a magnetic position sensor, which is fitted at a distal end of the guidewire and is configured to produce signals indicative of a position of the distal end; and an ultrasound (US) transducer, which is fitted at the distal end of the guidewire and is configured to transmit US waves inside the blood vessel, and acquire respective US echoes indicative of blood velocity in the blood vessel.
2. The medical probe according to claim 1, wherein the guidewire, the magnetic position sensor and the US transducer jointly have a maximal diameter that does not exceed 3.0 mm.
3. The medical probe according to claim 1, wherein the US transducer is configured to transmit the US waves in a distal direction and receive the US echoes from the distal direction.
4. The medical probe according to claim 1, wherein the US transducer is configured to transmit the US waves in a proximal direction and receive the US echoes from the proximal direction.
5. The medical probe according to claim 1, wherein the magnetic position sensor is formed on a flexible printed-circuit-board wrapped around the distal end of the guidewire.
6. A medical system, comprising: a guidewire ultrasound (US) probe comprising: a guidewire for insertion into a blood vessel of a patient; a magnetic position sensor, which is fitted at a distal end of the guidewire and is configured to produce signals indicative of a position of the distal end; and an ultrasound (US) transducer, which is fitted at the distal end of the guidewire and is configured to transmit US waves inside the blood vessel, and acquire respective US echoes indicative of blood velocity in the blood vessel; and a processor, which is configured to: receive from the US transducer electrical signals indicative of a Doppler shift of the echoes due to blood velocity; analyze the electrical signals to derive the blood velocity; and display the derived blood velocity to a user.
7. The medical system according to claim 6, wherein the guidewire, the magnetic position sensor and the US transducer jointly have a maximal diameter that does not exceed 3.0 mm.
8. The medical system according to claim 6, wherein the US transducer is configured to transmit the US waves in a distal direction and receive the US echoes from the distal direction.
9. The medical system according to claim 6, wherein the US transducer is configured to transmit the US waves in a proximal direction and receive the US echoes from the proximal direction.
10. The medical system according to claim 6, wherein the processor is configured to spectrally analyze the electrical signals to determine a maximal Doppler shift.
11. A manufacturing method, comprising: fitting a magnetic position sensor at a distal end of a guidewire for insertion into a blood vessel of a patient; fitting an ultrasound (US) transducer to a distal end of the guidewire; and wiring the magnetic position sensor and the US transducer.
12. A method, comprising: inserting a guidewire into a blood vessel of a patient, the guidewire having a magnetic position sensor and an ultrasound (US) transducer fitted at a distal end thereof, wherein the magnetic position sensor is configured to acquire position signals, and wherein the US transducer is configured to transmit US waves inside the blood vessel, and acquire respective US echoes indicative of blood velocity in the blood vessel; and navigating the guidewire to a target location in the blood vessel using signals acquired by the magnetic position sensor; at the target location, receiving from the US transducer electrical signals indicative of a Doppler shift of the echoes due to blood velocity; analyzing the electrical signals to derive the blood velocity; and displaying the derived blood velocity to a user.
13. The method according to claim 12, and comprising retracting the guidewire out of the blood vessel of the patient.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0015]
[0016]
[0017]
[0018]
[0019]
DETAILED DESCRIPTION OF EMBODIMENTS
Overview
[0020] An invasive probe comprising an ultrasound (US) transducer at its distal end may be inserted into a blood vessel to measure velocity of blood that flows in the vessel using the Doppler effect. The US reflecting media in blood are the red blood cells, and ultrasound waves reflected from the red blood cells (i.e., US echoes) change in frequency according to blood velocity relative to the US beam direction.
[0021] When the dominant direction of blood flow is exactly towards (or exactly away from) an US beam emitted by the transducer, the echoes gain a maximal positive (or negative) frequency shift compared to the frequency of the emitted US waves. Blood velocity, V.sub.B, can be derived from the maximal Doppler frequency shift, Δf, via the equation V.sub.B=V.sub.USΔf/f, where V.sub.US is the velocity of the US wave in blood and f is the US frequency. Since the Doppler effect is small, Δf may be estimated using spectral (e.g., Fourier) analysis of an echo signal acquired using sequences of pulsed US waves.
[0022] In practice, however, careful preparation of the intravascular measurement may be required, for example including, fixating the blood vessel walls to have well-defined blood flow profile. Such preparations can complicate the device and usage of an intravascular US blood velocity measurement method.
[0023] Embodiments of the present invention that are described hereinafter provide an ultrathin guidewire with a miniature US transducer fitted at its distal edge. The miniature US transducer is configured to emit US waves mainly at a distal and/or a proximal direction. The ultrathin guidewire and miniature transducer enable, and maintain, a largely laminar flow of the blood in the vicinity of the distal end. The transducer is configured to either emit ultrasound continuously or in pulses (A-mode), i.e., it is not an imaging transducer. The US transducer may comprise, for example, a miniature piezoelectric transceiver. A processor determines blood velocity based on analysis of the received echoes.
[0024] In some embodiments, the disclosed guidewire comprises a magnetic position sensor at its distal end, which is used to track a location of the distal end in the blood vessel where blood velocity is determined. The magnetic position sensor may comprise a single-, double-, or triple-axis magnetic transducer. The position of the distal end may be tracked, for example, using a magnetic position tracking system, such as the CARTO® system (made by Biosense-Webster, Irvine, Calif.).
[0025] In some embodiments, in order to fit the very small diameter guidewire the magnetic position sensor is formed on a flexible printed circuit board (PCB) wrapped around the ultrathin guidewire. An example of a magnetic position sensor formed on a flexible PCB, which is wrapped around a distal end of a sheath of a catheter, is described in U.S. patent application Ser. No. 16/248,393, filed Jan. 15, 2019, entitled “Position Sensor on Brain Clot Sheath and Location Pad Collar,” which is assigned to the assignee of the present patent application and whose disclosure is incorporated herein by reference.
[0026] In some embodiments, the maximal diameter of the US guidewire, including the US transducer and magnetic position sensor, does not exceed outer diameter (OD) of 3.0 mm.
[0027] The disclosed ultrathin US guidewire may be used to characterize blood flow before advancing a full-diameter catheter into a location in question, and may thereby simplify brain catheterization procedures.
System Description
[0028]
[0029] In some embodiments, prior to performing the disclosed diagnostic procedure, CT images of a patient 32 are acquired. The CT images are stored in a memory 42 for subsequent retrieval by a processor 40. The processor uses the CT images to present, for example, brain section image 59 demonstrating a blood vessel 48 in question on a monitor 56.
[0030] System 10 comprises a hollow guidewire 20, wherein a distal end of hollow guidewire 20 is inserted into patient 32 through a sheath 28, through an entry point 22 at an artery of a thigh of patient 32. Physician 54 navigates the distal end of hollow guidewire 20 through arteries to a brain location in question where blood velocity is to be measured.
[0031] To manipulate guidewire 20, physician 54 uses a controller handle 29, which is connected to the proximal end of hollow guidewire 20. The proximal end of controller handle 29 is coupled to a cable 19 that, in turn, is connected to a control console 50, to receive signals from sensors fitted at the distal end of guidewire 20.
[0032] During navigation, the position of a US transducer 60, which is fitted at a distal edge of hollow guidewire 20, is tracked using a magnetic tracking sub-system 23, which tracks position coordinates of magnetic sensor 25 fitted at the distal end of hollow guidewire 20.
[0033] Sub-system 23 comprises a location pad 24 that is fixed to the bed, and is fitted with magnetic field radiators 26 which are fixed in position relative to the head of patient 32 and which transmit alternating sinusoidal magnetic fields into a region 30 where the head of patient 32 is located. In response, magnetic sensor 25 generates position signals that are received by console 50.
[0034] During the procedure, the head of patient 32 is harnessed to keep it motionless. A location tracking system using a location pad similar to location pad 24 is described in U.S. patent application Ser. No. 15/674,380, filed Aug. 10, 2017,entitled “ENT Image Registration,” which is assigned to the assignee of the present patent application and whose disclosure is incorporated herein by reference with a copy provided in the Appendix.
[0035] Control console 50 comprises a processor 40, typically a general-purpose computer, with suitable front end and interface circuits (not shown) for receiving the US and position signals, as well as for controlling other components of system 10. Typically, processor 40 is configured to receive multiple measurements from US transducer 60 and to use these measurements to calculate blood velocity at the location of transducer 60.
[0036] Processor 40 uses software stored in a memory 42 to operate system 10. The software may be downloaded to processor 40 in electronic form, over a network, for example, or it may, alternatively or additionally, be provided and/or stored on non-transitory tangible media, such as magnetic, optical, or electronic memory. In particular, processor 40 runs a dedicated algorithm that enables processor 40 to perform the steps disclosed in
Guidewire US Probe for a Minimally Perturbing Measurement of Blood Flow in Brain Vessel
[0037]
[0038] US transducer 60, which is attached (64) to the distal edge of hollow guidewire 20, is navigated to a target location inside vessel 48 using magnetic position tracking sub-system 23 that tracks the location of magnetic position sensor 25. In the shown embodiment, US transducer 60 has an elongated shape so as not to disrupt blood flow. US transducer 60 is configured to emit US waves in a largely distal direction 66 parallel to a longitudinal axis 62 of distal end 30, and to receive Doppler shifted echoes 67 reflected from blood. However, other configurations are possible, in which, for example, transducer 60 is further configured to also emit US waves in a largely proximal direction and receive echoes from that direction. Typically, the lateral dimension of transducer 60 is up to 3.0 mm in diameter. The small dimension is enabled in part, due to transducer 60 being an A-mode transducer, in an embodiment.
[0039] In an embodiment, transducer 60 is fixed (e.g., glued) to the distal end of guidewire 20 over a distal perimeter of the hollow guidewire (not shown). In some embodiments, the wall of hollow guidewire 20 is made of a thin-wall polyimide tube reinforced with a metal coil. In an embodiment, the polyimide wall, or another suitable plastic, includes a braided coil of metal wire that serves to stiffen guidewire 20 while not limiting maneuverability.
[0040] As further seen, magnetic position sensor 25 is tightly wrapped around distal end 30, and glued together with its electrical leads (not shown). As noted above, in some embodiments, in order to conform with the small diameter guidewire, the magnetic position sensor is formed on a flexible printed circuit board (PCB) wrapped around ultra-thin hollow guidewire 20.
[0041] The example illustration shown in
[0042]
[0043] As seen, spectrum 68, despite being smoothed by the processing algorithm, has complex features and is continuous between a negative cutoff Doppler frequency denoted −Δf and a positive cutoff Doppler frequency denoted +Δf. The reason for this shape is that, in practice, US echoes of variable strengths are received from multiple directions and not only from the distal and/or proximal ones. Yet, regardless of the shape of spectrum 68, processor 40 can accurately determine blood velocity, V.sub.B, by estimating the cutoff values of the Doppler shift, −Δf and +Δf, and calculating V.sub.B using the aforementioned equation for blood velocity, V.sub.B=V.sub.USΔf/f.
[0044]
[0045] Next, at a transducer gluing manufacturing step 72, transducer 60 is glued (64) to hollow guidewire 20 over a perimeter of the distal edge hollow reinforced guidewire 20. Alternatively, heat may be used to melt proximal perimeters of a plastic shell of transducer 60 to the exterior guidewire surface. Finally, at a magnetic position sensor disposing step 74, magnetic position sensor 25 is wrapped around distal end 30 of hollow guidewire 20, and glued together with its electrical leads (not shown).
[0046] The example flow-chart shown in
[0047]
[0048] Next, physician 54 uses system 10, including sensor 25, to navigate and position transducer 60 at a vessel 48 location in question, at a US transducer positioning step 82. Physician 54 then acquires Doppler shifted echoes, at a blood velocity measurement step 84.
[0049] The acquired US signals are processed by processor 40, which derives blood velocity at the location, at a blood velocity derivation step 86. Processor 40 displays the derived blood velocity to physician 54 on a monitor 56, at blood velocity displaying step 88.
[0050] Finally, physician 54 retracts transducer 60 from vessel 48 by pulling out hollow guidewire 20, at guidewire US probe retraction step 90.
[0051] Although the embodiments described herein mainly address cerebrovascular applications, the methods and systems described herein can also be used in other applications, such as in measuring blood velocity at any other sufficiently large blood vessel of the body.
[0052] It will be appreciated that the embodiments described above are cited by way of example, and that the present invention is not limited to what has been particularly shown and described hereinabove. Rather, the scope of the present invention includes both combinations and sub-combinations of the various features described hereinabove, as well as variations and modifications thereof which would occur to persons skilled in the art upon reading the foregoing description and which are not disclosed in the prior art. Documents incorporated by reference in the present patent application are to be considered an integral part of the application except that to the extent any terms are defined in these incorporated documents in a manner that conflicts with the definitions made explicitly or implicitly in the present specification, only the definitions in the present specification should be considered.