WO2003013624A2 - Intra vascular imaging method and apparatus - Google Patents

Intra vascular imaging method and apparatus Download PDF

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Publication number
WO2003013624A2
WO2003013624A2 PCT/IL2002/000659 IL0200659W WO03013624A2 WO 2003013624 A2 WO2003013624 A2 WO 2003013624A2 IL 0200659 W IL0200659 W IL 0200659W WO 03013624 A2 WO03013624 A2 WO 03013624A2
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WO
WIPO (PCT)
Prior art keywords
catheter
image
blood
distal end
fluid
Prior art date
Application number
PCT/IL2002/000659
Other languages
French (fr)
Other versions
WO2003013624A3 (en
Inventor
Doron Adler
Alex Zaretski
Ofer Pillar
Keren Shafrir
Mordechai Segev
Sharon Ehrlich
Original Assignee
C2Cure Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by C2Cure Inc. filed Critical C2Cure Inc.
Priority to AU2002324316A priority Critical patent/AU2002324316A1/en
Priority to EP02758761A priority patent/EP1465684B1/en
Priority to IL15982902A priority patent/IL159829A0/en
Priority to CA002456418A priority patent/CA2456418A1/en
Priority to JP2003518624A priority patent/JP4471651B2/en
Publication of WO2003013624A2 publication Critical patent/WO2003013624A2/en
Priority to IL159829A priority patent/IL159829A/en
Publication of WO2003013624A3 publication Critical patent/WO2003013624A3/en

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/313—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor for introducing through surgical openings, e.g. laparoscopes
    • A61B1/3137—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor for introducing through surgical openings, e.g. laparoscopes for examination of the interior of blood vessels
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00064—Constructional details of the endoscope body
    • A61B1/00071—Insertion part of the endoscope body
    • A61B1/0008—Insertion part of the endoscope body characterised by distal tip features
    • A61B1/00082—Balloons
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00064—Constructional details of the endoscope body
    • A61B1/00071—Insertion part of the endoscope body
    • A61B1/0008—Insertion part of the endoscope body characterised by distal tip features
    • A61B1/00091—Nozzles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00163—Optical arrangements
    • A61B1/00193—Optical arrangements adapted for stereoscopic vision
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/012—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor
    • A61B1/015—Control of fluid supply or evacuation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/06—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
    • A61B1/0655—Control therefor
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/02007—Evaluating blood vessel condition, e.g. elasticity, compliance
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/04—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances
    • A61B1/05—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances characterised by the image sensor, e.g. camera, being in the distal end portion
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/06—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
    • A61B1/0638—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements providing two or more wavelengths
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/0059—Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence
    • A61B5/0082—Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence adapted for particular medical purposes
    • A61B5/0084—Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence adapted for particular medical purposes for introduction into the body, e.g. by catheters
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/026—Measuring blood flow
    • A61B5/0275—Measuring blood flow using tracers, e.g. dye dilution
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S977/00—Nanotechnology
    • Y10S977/84—Manufacture, treatment, or detection of nanostructure
    • Y10S977/849—Manufacture, treatment, or detection of nanostructure with scanning probe
    • Y10S977/86—Scanning probe structure
    • Y10S977/868—Scanning probe structure with optical means
    • Y10S977/869—Optical microscope
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S977/00—Nanotechnology
    • Y10S977/84—Manufacture, treatment, or detection of nanostructure
    • Y10S977/849—Manufacture, treatment, or detection of nanostructure with scanning probe
    • Y10S977/86—Scanning probe structure
    • Y10S977/875—Scanning probe structure with tip detail
    • Y10S977/876—Nanotube tip

Definitions

  • the present invention relates to an intra vascular imaging method
  • cavities of the body including methods and apparatus for visualization through
  • Atherosclerotic plaques which are an active collection of different cells, mainly
  • plaques otherwise known as vulnerable plaques. This type of plaque is usually
  • the commonly applied method, angiography includes
  • occlusions in small blood vessels of other organs such as the brain, kidney, or
  • intra- vascular imaging such as in the present invention
  • intra- vascular imaging are angioscopy and intra-luminal ultrasound.
  • Angioscopy is a form of endoscopy developed for the arteries. Because
  • the illumination used in angioscopy is in the visible wavelength range, in which
  • the method requires a way of moving
  • angioscope in front of the camera-head or optical assembly.
  • the balloon is
  • distal end of the angioscope and clears a field of view of the walls of the vessel.
  • Another method for intra-vascular imaging is the use of ultrasound.
  • ultrasound transducer is positioned at the distal end of a catheter inside the
  • Patents referring to this kind of apparatus are
  • ultrasonic imaging is US5167233.
  • OCT provides a three-dimensional image by performing optical
  • a well-known property of human tissue is that it has different absorption
  • an invasive imaging apparatus comprising;
  • a flexible catheter with a proximal end and a distal end, said distal
  • At least one working channel running from the proximal to the distal
  • said illumination source utilizes at least one wavelength taken
  • said illumination source uses at least one wavelength
  • said illumination source is comprised of an infra-red
  • illumination source positionable outside of said patient's body.
  • illumination source is controllable to be aimed directly at
  • said illumination source is controllable to be directed in a
  • said optical assembly comprises optical components and an
  • said imaging assembly comprises said image sensor and an
  • optical components comprise a lens with two optical
  • said light deflector is one of a prism and a mirror with a
  • said image sensor and said illumination sensor are operable
  • infra-red light to correspond to said illumination source.
  • a polarized filter is positionable before at least one of a
  • said working channel comprises a guide wire.
  • said working channel is usable for controllably passing
  • said image sensor is positioned substantially parallel to the
  • said image sensor is shaped to fit within restricted
  • said image sensor is a CMOS or CCD-based pixel sensor.
  • said image sensor comprises an imaging area shaped in a
  • Preferably said rectangular pixel array measures 128 x 256 pixels.
  • said sensor comprises sensor control electronic circuitry
  • imaging area located beneath a shorter side of said imaging area, said imaging area being
  • I/O and supply pads for said electronic circuitry are placed
  • said display and control unit is operable to control the timing
  • a transparent balloon-like structure is positioned at said distal
  • said balloon-like structure is rigid
  • said balloon-like structure is flexible.
  • said balloon-like structure is inflated and deflated by means
  • said optical assembly comprises two image sensors for
  • the injection of said fluid is synchronized with the operation
  • one of said physiological conditions is heart beat sensible
  • a heart rate sensor such as a plethysmograph, or other device
  • central control unit enabling synchronization with said physiological
  • said balloon-like structure is pressure-sensed to provide real ⁇
  • said working channel is usable for passage of therapeutic
  • optical assembly is used in conjunction with a laser
  • said laser cutting device to enable laser operated surgery.
  • said laser cutting device is used to obtain biopsy biological
  • optical assembly and said laser cutting device are used in
  • an invasive imaging control apparatus comprising:
  • a flexible catheter with a proximal end and a distal end, said distal
  • An optical assembly positioned at the distal end of said catheter.
  • At least one working channel running from the proximal to the distal
  • said optical assembly comprises an illumination sensor
  • said working channel is usable for controllably passing
  • control unit is connectable to the proximal end of said
  • control unit is operable to control the timing and amount
  • the injection of said fluid is synchronized with the operation
  • said fluid is insertable into the immediate region of said distal
  • said fluid comprises one or more fluids selected to modify the
  • said physiological condition is heart beat sensible using a
  • heart rate sensor (such as a plethysmograph, or other device) connectable to a
  • central control unit enabling synchronization with said physiological
  • invasive imaging control apparatus comprising: a. A flexible catheter with a proximal end and a distal end, said distal
  • An optical assembly positioned at the distal end of said catheter.
  • At least one working channel running from the proximal to the distal
  • a semi-permeable membrane positioned at said distal end of said
  • said membrane is rigid.
  • said membrane is flexible.
  • said membrane is inflated and deflated by means of
  • the injection of said fluid is synchronized with the operation
  • one of said physiological conditions is heart beat sensible
  • a heart rate sensor such as a plethysmograph, or other device
  • central control unit enabling synchronization with said physiological
  • optical assembly temporarily changing the optical characteristics of the blood
  • optical assembly temporarily changing the reflectance of the liquid portion of
  • said fluid being a
  • physiological fluid such as saline
  • hypoosmolar fluid such as 0.45%
  • said fluid being a blood
  • said fluid is chosen to enable illumination to facilitate
  • said fluid is chosen to be oxygen carrying, such as a blood
  • vasculature or other organs based on image data from both said longitudinal
  • said off-line image training initialization comprises:
  • training image is clipped and rotated to obtain robust
  • said local contrast enhancement comprises:
  • said first image is produced by modifying the intensity of
  • said real-time data inte ⁇ olation comprises:
  • a preferred embodiment comprises generating said set of direction
  • Fig. 1 is a simplified schematic of the overall patient system.
  • Fig. 2 A is a simplified schematic of the optical head — side view.
  • Fig. 2B is a simplified schematic of the optical head — top view.
  • Fig. 3 is a system block diagram.
  • Fig. 4A is a simplified schematic of the optical array assembly.
  • Fig. 4B is a schematic example configuration of optical design A.
  • Fig 4C is a schematic example configuration of optical design B.
  • Fig. 5A is a simplified diagram of a configuration with the optical head
  • Fig. 5B is a simplified diagram of a configuration with the optical head
  • Fig. 6 is a schematic representation of the image sensor.
  • Fig. 7 is a block diagram of the post-processing algorithm.
  • Fig 8 is a simplified schematic of use of an external IR source.
  • Fig 9 is a simplified schematic of a biological sample collector.
  • a small-diameter flexible catheter with a distal end that can be
  • a viewing apparatus which is positioned at the distal end of the
  • catheter and consists of a specifically designed image sensor, a distorting
  • optical assembly and an illumination source.
  • the image sensor is shaped to fit within the restricted dimensions of
  • the image sensor is positioned non-peipendicularly to the
  • the catheter to contain both the viewing apparatus and a working channel
  • the optical assembly is designed to distort and deflect the light
  • the light source or sources may be visible light sources, IR sources
  • the lighting is either aimed directly at the imaged object
  • One or more working channels which run along the length of the
  • a channel for a guide wire is necessary, and may be provided as
  • the local area network is conducted through a wire connection or a wireless connection.
  • controller may be an entirely separate element situated at the distal head of the
  • catheter as described above, but it also may be a part of the image sensor.
  • a central control and display unit is typically located on a rack in the
  • This unit executes, among other tasks, basic
  • a device only or as part of a PTCA, stenting, laser, or any other operative device.
  • operative devices is by mounting the viewing apparatus at the distal end of a
  • the guide wire is inserted into the artery at the beginning of a
  • Fig. 1 is a simplified schematic of the
  • the configuration has a processing and control unit
  • digital video unit 40 comprising, among others, three functional units: digital video unit 40;
  • balloon inflation unit 41 balloon inflation unit 41; and fluid injection unit 42.
  • catheter 30 is connected to the processing and control unit 28.
  • the display unit 28 controls the processing and control unit 28.
  • the catheter 30 is inserted into the patient 25 with the inflatable balloon 31 located at the catheter distal end, inside the patient.
  • a heart rate sensor 26 is
  • the heart rate of the patient 25 is monitored either by a heart rate sensor
  • heart rate is sent to the processing and control unit 28.
  • the processing and control unit 28 The processing and control unit 28.
  • control unit receives the information, processes it and synchronizes the
  • the catheter 30 is connected to the
  • FIG. 2A and 2B are schematic details of
  • the optical head comprises a lens 2 and an optical
  • the illumination sensor 1 and an image sensor 8 (for acquiring images).
  • image sensor 8 may be separate elements or they may be combined
  • One or more illumination sources 3 which may use visible or infrared
  • pressure sensor 7 is also positioned at the distal end of the optical head.
  • a variable volume transparent balloon 6 encloses all components on the distal
  • a mechanical enclosure houses the previously mentioned components and
  • variable volume transparent balloon 6 serves as the proximal surface of the variable volume transparent balloon 6.
  • Working channel A 4 representing one or more such channels, runs along the
  • catheter 30 and terminates at the distal end inside of the variable volume
  • a cable 5 runs along the catheter 30 and
  • the illumination sources 3 in the present embodiment illuminate the
  • Working channels (in this example, two)
  • variable volume transparent balloon 6 6.
  • variable volume transparent balloon 6 enables short period imaging
  • variable volume transparent balloon pressure is sensed and
  • the system has a fixed optical
  • transparent balloon 6 has known optical attributes and it enables close contact with the blood vessel wall. Inflation of the variable volume transparent balloon
  • variable volume transparent balloon 6 When deflated, the variable volume transparent balloon 6 allows an
  • variable volume transparent balloon 6 is inflated again.
  • a safety mechanism comprising
  • a pressure sensor 7 ensures that pressure within the balloon is maintained at
  • a local controller 11 coordinates data flow to and from the optical
  • FIG. 3 highlights the logic in and between the optical head 20, as detailed in
  • the local processor 11 serves to control the functions of the optical head 20
  • optical head 20 located in the operating room. Functions of the optical head 20 are the
  • illumination source 3 (commanded by the local processor 11), light sensor 8
  • image sensor 1 (which feeds back to the local processor 11), image sensor 1 (which feeds back to the local processor 11), image sensor 1 (which feeds back
  • the local processor 11 receives and sends commands and receives power from the video control and command unit 40 and power and data control
  • command unit 13 together form the core of command and control of the entire
  • supply controller 14 power supply to power
  • controller 41 operates through working channel A 4, which physically passes
  • air pressure control 41 commands the physiological fluid control source 42.
  • the suction mechanism 19 and laser source 18 all function through working
  • channel B 9 which runs along the catheter but parallel and external to the
  • the suction mechanism 19 and laser source 18 are devices that are
  • the local processor 11 controls and coordinates functioning of
  • power and data control unit 13 include, timing control of the system functions
  • optical distortion created by the image sensor 1 taking into account the system overall design are controlled by the video control and command unit 40.
  • Images processed by the video control and command unit 40 may be
  • the first modality is a succession of separate
  • the second modality is a stream of video images.
  • processing and control unit 28 performs a time
  • the optical array assembly 48 is comprised of a lens 2
  • the prism 22 is positioned above the image sensor 1.
  • One preferred prism is positioned above the image sensor 1.
  • embodiment consists of a lens 2 with two optical planes, a shutter 12 and a
  • the optical array assembly 48 is
  • the lens 2 and prism 22 are two fixed optical components
  • PMMA refers to a specific plastic lens material called polymethyl
  • Figure 5 A shows an
  • an optical head 47 is located distally to the PTCA/stent
  • the stent balloon 50 is located distally to the catheter 30.
  • optical head 47 is located within a second balloon 60.
  • a regulating valve 55 is
  • Inflation of the second balloon 60 is enabled by the regulating valve 55, which
  • multiple light sources on board light receivers, and an on board pressure sensor
  • the regulating valve 55 is designed to close itself
  • valve closes and the PTCA/stent balloon 50 inflates.
  • the second balloon 60 inflates the second balloon 60, made of a transparent membrane which is non-
  • the regulating valve 55 also controls
  • Figure 5B shows an embodiment where the optical head 48 is installed
  • the optical head assembly is distally and exterior to the PTCA/stent balloon 50.
  • the PTCA/stent balloon 50 is located at the distal end of the catheter. Note
  • optical head assembly 48 shown in Figure 5B is similar to the optical
  • a regulating valve 56 located distally to the PTCA/stent balloon
  • Each cycle comprises a delay after which fluid is
  • injection are synchronized and timed so that they occur after a pulse of blood
  • the regulating valve 56 is opened and fluid is
  • optical head assembly 48 and power dissipation of the light source.
  • the sensor comprises an imaging area 71 which
  • the sensor is shaped as a rectangle pixel area, such as a 128 x 256 pixel array.
  • circuitiy 72 may also contain additional circuitiy 72 that performs functions such as analog
  • Supply pads 73 are
  • the sensor 70 is located in the optical head assembly previously
  • the sensor 70 serves to capture the
  • the senor is positioned non-pe ⁇ endicularly to
  • the longitudinal axis of the catheter In a preferred embodiment it is placed
  • the small width of the imaging area makes it possible to
  • Figure 7 is a simplified block
  • the central control and display unit has been received by the central control and display unit.
  • control and display unit is preferably located in the operating room, and it
  • the catheter preferably located in a blood vessel.
  • the initialization and training sequence 301 takes place as a one-time
  • the aim of this sequence is to determine the optimal set of
  • pre input image conversion 303 takes
  • the training process is
  • Real-time execution begins with step 306, when a new image is received
  • the next step is to find the direction for each pixel 308 in the intensity
  • the first step of contrast enhancement is to perform image segmentation
  • Enhancement function is a function of the average intensity and the local
  • near-IR light may be advantageous
  • IR light may be used in a viewing apparatus designed for intra-vascular
  • the apparatus and method in the present embodiment includes a
  • the previously mentioned imaging sensing apparatus is applicable to the
  • the apparatus consists of one or more light sources which
  • the image sensor is preferably a CMOS or CCD pixilated sensor.
  • the senor may use filters that have
  • CMOS complementary metal-oxide-semiconductor
  • CCD complementary metal-oxide-semiconductor
  • the light sources may also include a combination of wavelengths of
  • IR light can be used in another diagnostic embodiment, considering the
  • the present embodiments can include an analyzing apparatus for the analysis of these coefficients. Evaluation of blood status (for example, sugar level in the
  • blood may be analyzed by evaluating the IR light absorption) may be one of the
  • Another embodiment uses external IR illumination. Reference is made to
  • the optical assembly 80 is located at the distal end of the catheter 30
  • the function of on- light receiver is preferably included.
  • the function of on- light receiver is preferably included.
  • the light source is not on board the optical head assembly
  • blood may be temporarily diluted at the site of an object to be imaged.
  • the injection fluid is not necessarily a physiological fluid.
  • the present embodiment includes a
  • a working channel through which the fluid may be injected from the proximal
  • measurement may supply the timing to inject the physiological fluid into the
  • the reflected light measurement may provide for
  • a quality control algorithm which may be able to calculate necessary changes to lighting or fluid injection from the received image to improve image
  • concentration of particles such as 1/6 saline.
  • concentration of particles such as 1/6 saline.
  • Another embodiment uses a fluid that is capable of carrying oxygen
  • This embodiment uses a transparent dome or balloon, either
  • the structure is positioned at the distal end of the catheter,
  • a flexible balloon which inflates by injecting a transparent fluid or gas into it. It is positioned at the distal end of the catheter at its deflated mode.
  • injection is preferably, centrally controlled and the fluid or gas may be injected
  • the balloon displaces the blood from the field of view, as does the
  • the structure is a
  • the rigid structure extends distally to it.
  • the rigid structure is situated so that it removes the blood
  • rigid structure is either hollow (vacuum, gas) or filled with a transparent fluid.
  • Light that impinges on a surface has a component that returns polarized.
  • Reflected light is more polarized when the incidence angle is closer to normal.
  • Imaged objects are
  • a distal balloon made of a transparent membrane blocking the
  • the injected fluid can also be used for the
  • This embodiment enables an accurate operation
  • Another embodiment is that of biopsy and sample retrieval.
  • Working channel B 9 is used to pass
  • optical head 90 to enable visual inspection of the desired location.
  • Samples may be transferred through the working channel B 9
  • the optical head 90 is used to hold a sample in position and the laser apparatus is used to cut the sample from surrounding tissue.
  • the optical head 90 is
  • suction/nano-gripper 99 and laser device 98 can alternately or
  • Minimally invasive surgery is

Abstract

An invasive imaging apparatus comprising: a flexible catheter (30) with a proximal end and a distal end, the distal end being shaped for insertion into a blood vessel along a guide wire (9) thereby to reach remote places in the vasculature or other organs, an optical assembly positioned at the distal end of the catheter comprising an image sensor (10) positioned non-perpendicularly to the longitudinal axis of the catheter, at least one illumination source (3) for illuminating an immediate region beyond the distal end of the catheter, and at least one working channel (4) running from the proximal to the distal end of the catheter.

Description

INTRA VASCULAR IMAGING METHOD AND APPARATUS
FIELD AND BACKGROUND OF THE INVENTION
The present invention relates to an intra vascular imaging method and
apparatus which allow the acquisition of endoscopic images of small internal
cavities of the body including methods and apparatus for visualization through
opaque liquid media.
Heart and blood vessel diseases are among the main causes for morbidity
and mortality in Western society. Therefore, interventional procedures
involving blood vessels of the heart are among the most widely used in the
medical field. The pathology that is in the base of most acute coronary
syndromes and sudden cardiac deaths is atherosclerosis. In this process,
atherosclerotic plaques, which are an active collection of different cells, mainly
immune cells and smooth muscle cells along with deposits of fatty substances,
cholesterol, cellular waste products, calcium and other substances, are
accumulated in the inner lining of an artery. Stable plaques, which cause the
more significant narrowing of the arterial wall, are considered the major factor
in the development of angina pectoris (chest pain). However, studies from
recent years have shown, that unstable angina, myocardial infarctions (heart
attacks) and sudden cardiac related deaths are caused mainly by unstable
plaques, otherwise known as vulnerable plaques. This type of plaque is usually
smaller and therefore less significant and difficult to detect with currently used
angiographic methods described hereafter. Some of the important developments were made in the field of minimally
invasive procedures. A very common diagnostic and therapeutic procedure is
cardiac catheterization. The commonly applied method, angiography, includes
imaging the heart and coronaiy blood vessels using an X-ray camera as the
imaging device, and a catheter, through which a contrast substance is injected
into the heart and vessels to enable them to be viewed by the camera. This
method gives a two-dimensional monochromatic view of the heart and blood
vessels as viewed from the outside. This method detects major occlusions by
identifying places where blood flow is disturbed and it may direct the PTCA
(Percutaneous Transluminal Coronary Angioplasty) or stent-inserting technique
to the place of the occlusion, but it does not give a direct view of the occlusion
site or the surrounding area. One of the major risks of the techniques described
above is a rupture or a disruption in the fibrous cap covering the plaque and the
release of plaque particles into the blood stream. These particles may cause
numerous small occlusions in the coronary arteries but also may cause
occlusions in small blood vessels of other organs, such as the brain, kidney, or
lungs. A direct, clear view of the field of operation, as provided in the current
invention, could substantially decrease the risk of disruption, as described
above. Also, and perhaps more importantly, only through intra- vascular
imaging will it be possible to detect the smaller, vulnerable plaques. The
effectiveness and precision of the plaque treatment, when assisted with direct
intra- vascular imaging, such as in the present invention, would be enhanced
when compared to current indirect imaging methods. Important methods that have been developed to confront the issue of
intra- vascular imaging are angioscopy and intra-luminal ultrasound. New
techniques, which are still under development, include Optical Coherence
Tomography (OCT) and infrared endoscopy.
Angioscopy is a form of endoscopy developed for the arteries. Because
the illumination used in angioscopy is in the visible wavelength range, in which
the blood that fills the arteries is opaque, the method requires a way of moving
the blood from the field of view prior to visualization. One way to do this is by
injecting a high-pressure physiological fluid into the vessel to temporarily
displace the blood, as disclosed in patents US4827907, US4998972,
US5730731, US5010875 and US4934339. Another way of clearing the field of
view is by inflating a balloon, which is positioned at the distal end of the
angioscope, in front of the camera-head or optical assembly. The balloon is
made of a transparent substance, so that when it is inflated inside the blood
vessel, with either gas or a transparent liquid, it pushes the blood away from the
distal end of the angioscope and clears a field of view of the walls of the vessel.
Such an apparatus is described in US4784133 and US5411016; the latter patent
disclosing a transparent part at the distal end of the angioscope in addition to
the balloon surrounding it. A similar apparatus is disclosed in US4470407,
except that the optical system terminates inside the balloon (also allowing laser
operation through the balloon). An apparatus that uses two spaced and
expendable balloons, that occlude and isolate an operating area in the blood
vessel between them, is disclosed in US4445892. Most methods combine an inflatable balloon with injection of a transparent liquid. The balloon coaxially
surrounds the sheath at the distal end of the catheter and, when inflated, it
blocks some of the blood flow. The method described above allows the
injection of less flush liquid and at a lower pressure, which is safer and more
efficient. Prior art in which the method described above is used is US4576145,
US4576146, US5263928 and US5464394. A combination of an angioplasty
balloon with intra- vascular endoscopy is disclosed in patents EP 177124 A,
US5116317 and US4961738. In the latter patent, the optical system terminates
within the balloon and there is a "working well" in the balloon to allow the
insertion of instruments into the lumen of the vessel.
Another method for intra-vascular imaging is the use of ultrasound. The
ultrasound transducer is positioned at the distal end of a catheter inside the
blood vessel and the ultrasound transducer is used to obtain an image of the
lumen and walls of the artery. Patents referring to this kind of apparatus are
US6129672, US6099475, US6039693, US6059731, US5022399, US4587972,
US4794931, US4917097 and US5486170. A patent that combines PTCA with
ultrasonic imaging is US5167233.
OCT provides a three-dimensional image by performing optical
measurements, and it can be used in intra-vascular imaging. Related patents
are US6134003, US6010449, and US5459570.
The opaqueness of blood at visible light wavelengths poses a specific
problem when attempting to acquire an image of an intra-vascular space. One
solution to the problem noted above is to utilize infrared (IR) light to enable visibility through the suspended particles and cells in the blood. A patent that
discloses a method for using deep-IR light for imaging through blood is
US6178346. The use of deep-IR wavelengths to achieve visibility in a blood
medium as described in the referred patent requires very high-energy
illumination, which has risks and disadvantages when used inside the body.
The use of near-IR radiation substantially diminishes risks. US4953539
discusses the use of an endoscopic imaging device, which is illuminated from
outside the body with infrared light. The referred patent serves as an example
of the use of infrared light in imaging body organs. External illumination has
not been used to date for intra-vascular imaging.
A well-known property of human tissue is that it has different absorption,
scattering, and attenuation coefficients of IR radiation. This fact allows
different types of tissues to be distinguished in general, and allows different
types of plaque to be to be distinguished in particular. Reference is made to "A
Review of the Optical Properties of Biological Tissues" Cheong, Prahl and
Welch, IEEE J. of Quantum Electronics, Nol 26 o 12 December 1990.
SUMMARY OF THE INVENTION
According to a first aspect of the present invention there is thus provided
an invasive imaging apparatus comprising;
a. A flexible catheter with a proximal end and a distal end, said distal
end being shaped for insertion into a blood vessel along a guide wire
thereby to reach remote places in the vasculature or other organs.
b. An optical assembly positioned at the distal end of said catheter
comprising an image sensor positioned non-peφendicularly to the
longitudinal axis of said catheter.
c. At least one illumination source for illuminating an immediate
region beyond the distal end of said catheter.
d. At least one working channel running from the proximal to the distal
end of said catheter.
Preferably said illumination source utilizes at least one wavelength taken
from within a range comprising visible light, near infra-red, and infra-red light.
A preferred embodiment comprises a plurality of illumination sources
and said illumination sources are controlled together.
A preferred embodiment comprises a plurality of illumination sources
and said illumination sources are controlled separately.
Preferably said illumination source uses at least one wavelength
preselected to improve visibility through blood.
Preferably said illumination source is comprised of an infra-red
illumination source positionable outside of said patient's body. Preferably said illumination source is controllable to be aimed directly at
an imaged object from the direction of said imaging assembly.
Preferably said illumination source is controllable to be directed in a
general viewing direction.
Preferably said optical assembly comprises optical components and an
imaging assembly.
Preferably said imaging assembly comprises said image sensor and an
illumination sensor.
Preferably said optical components comprise a lens with two optical
planes, a shutter, and a light deflector.
Preferably said light deflector is one of a prism and a mirror with a
reflecting surface.
Preferably said image sensor and said illumination sensor are operable
to sense at least one wavelength taken from within a range from visible light to
infra-red light to correspond to said illumination source.
Preferably a polarized filter is positionable before at least one of a
member of a group comprising said illumination sensor, said image sensor, said
illumination sources, and said lens, and said polarized filter polarization
direction is controllable to enhance image quality.
A preferred embodiment comprises a central control and display unit
connectable to the proximal end of said catheter from outside of the patient's
body.
Preferably said working channel comprises a guide wire. Preferably said working channel is usable for controllably passing
through fluid to said distal end of catheter.
Preferably said image sensor is positioned substantially parallel to the
longitudinal axis of said catheter.
Preferably said image sensor is shaped to fit within restricted
dimensions of said catheter.
Preferably said image sensor is a CMOS or CCD-based pixel sensor.
Preferably said image sensor comprises an imaging area shaped in a
rectangular pixel array.
Preferably said rectangular pixel array measures 128 x 256 pixels.
Preferably said sensor comprises sensor control electronic circuitry
located beneath a shorter side of said imaging area, said imaging area being
arranged as a rectangular pixel array.
Preferably I/O and supply pads for said electronic circuitry are placed
along at least one of the shorter sides of said image sensor.
A preferred embodiment with a local controller located at the distal end
of said catheter to coordinate data flow to and from said optical assembly and
to perfoπn commands received from said central control and display unit.
Preferably said display and control unit is operable to control the timing
and amount of injection of said fluid.
Preferably a transparent balloon-like structure is positioned at said distal
end of said catheter to displace blood from around the optical sensor-head,
allowing clear visibility. Preferably said balloon-like structure is rigid
Preferably said balloon-like structure is flexible.
Preferably said balloon-like structure is inflated and deflated by means
of using a liquid or a gas passed through said working channel.
Preferably said optical assembly comprises two image sensors for
obtaining a stereoscopic image.
Preferably the injection of said fluid is synchronized with the operation
of said optical assembly, synchronizing said operation and said injection with
the cycle of patient physiological conditions.
Preferably one of said physiological conditions is heart beat sensible
using a heart rate sensor (such as a plethysmograph, or other device)
connectable to a patient's body from outside of said patient's body or insertable
into said blood vessel through said catheter.
Preferably information from said heart rate sensor is transferred to said
central control unit enabling synchronization with said physiological
conditions.
Preferably said balloon-like structure is pressure-sensed to provide real¬
time feedback when said balloon-like structure impinges upon an obstacle, such
as a blood vessel wall.
Preferably said working channel is usable for passage of therapeutic
instruments to a site of operation.
Preferably said optical assembly is used in conjunction with a laser
cutting device to enable laser operated surgery. Preferably said laser cutting device is used to obtain biopsy biological
samples by cutting and transferring through said working channel to the
proximal end of said catheter.
Preferably said optical assembly and said laser cutting device are used in
conjunction with one of a suction and nano-gripper mechanisms to enable
visual inspection of a desired location for biological sample retrieval.
According to a second aspect of the present invention there is provided
an invasive imaging control apparatus comprising:
a. A flexible catheter with a proximal end and a distal end, said distal
end being shaped for insertion into a blood vessel along a guide wire
thereby to reach remote places in the vasculature or other organs.
b. An optical assembly positioned at the distal end of said catheter.
c. At least one working channel running from the proximal to the distal
end of said catheter.
d. A control unit for regulating the opacity level of blood in said blood
vessel around said distal end of said catheter, controllably injecting
quantities of fluid into said blood vessel in the vicinity of said optical
assembly, thereby enhancing visibility.
Preferably said optical assembly comprises an illumination sensor
operable to sense at least one wavelength taken from within a range from
visible light to infra-red light.
Preferably said working channel is usable for controllably passing
through fluid to said distal end of catheter. Preferably said control unit is connectable to the proximal end of said
catheter from outside of the patient's body.
Preferably said control unit is operable to control the timing and amount
of injection of said fluid.
Preferably the injection of said fluid is synchronized with the operation
of said optical assembly, synchronizing said operation and said injection with
the cycle of patient physiological conditions.
Preferably said fluid is insertable into the immediate region of said distal
end of said catheter to change the optical characteristics of blood in said
immediate region.
Preferably said fluid comprises one or more fluids selected to modify the
optical characteristics of blood plasma to render said optical characteristics to
be as close as possible to those of red blood cells.
Preferably said physiological condition is heart beat sensible using a
heart rate sensor (such as a plethysmograph, or other device) connectable to a
patient's body from outside of said patient's body or insertable into said blood
vessel through said catheter.
Preferably information from said heart rate sensor is transferred to said
central control unit enabling synchronization with said physiological
conditions.
According to a third aspect of the present invention there is provided an
invasive imaging control apparatus comprising: a. A flexible catheter with a proximal end and a distal end, said distal
end being shaped for insertion into a blood vessel along a guide wire
thereby to reach remote places in the vasculature or other organs.
b. An optical assembly positioned at the distal end of said catheter.
c. At least one working channel running from the proximal to the distal
end of said catheter
d. A semi-permeable membrane positioned at said distal end of said
catheter, surrounding said optical assembly extendable to displace
blood from around the optical assembly allowing clear visibility.
Preferably said membrane is rigid.
Alternatively, said membrane is flexible.
Preferably said membrane is inflated and deflated by means of
controllably passing a fluid through said working channel to said distal end of
catheter.
A preferred embodiment has a control unit connectable to the proximal
end of said catheter from outside of the patient's body.
Preferably the injection of said fluid is synchronized with the operation
of said optical assembly, synchronizing said operation and said injection with
the cycle of patient physiological conditions.
Preferably one of said physiological conditions is heart beat sensible
using a heart rate sensor (such as a plethysmograph, or other device)
connectable to a patient's body from outside of said patient's body or insertable
into said blood vessel through said catheter. Preferably information from said heart rate sensor is transferred to said
central control unit enabling synchronization with said physiological
conditions.
According to a fourth aspect of the present invention there is provided a
method for performing biopsies and other diagnostic or therapeutic procedures
comprising placing an invasive optical assembly apparatus on the distal end of
a needle, inserting said optical assembly and needle into vasculature or other
organs, and using said optical assembly to provide visual feedback of said
biopsies and diagnostic or therapeutic procedures.
According to a fifth aspect of the present invention there is provided a
method for viewing through blood in Situ comprising injecting a controlled
amount of fluid into blood in the immediate region in front of an invasive
optical assembly, temporarily changing the optical characteristics of the blood
in said immediate region, and thereby improving visibility through said blood.
According to a sixth aspect of the present invention there is provided a
method for viewing through blood in Situ comprising injecting a controlled
amount of fluid into blood in the immediate region in front of an invasive
optical assembly, temporarily changing the reflectance of the liquid portion of
said blood, and improving visibility through said blood.
Preferably said fluid is used to change the optical characteristics of
blood in Situ to facilitate imaging through said blood, said fluid being a
physiological fluid, such as saline, or a hypoosmolar fluid, such as 0.45%
saline or 1/6 saline. Preferably said fluid for use in changing the optical properties of blood
in Situ to facilitate imaging through said blood, said fluid being a blood
substitute which does not contain red blood cells and has homogenous optical
characteristics.
Preferably said fluid is chosen to enable illumination to facilitate
imaging through said blood and the environment in Situ with an IR
illumination source, enabling a frequency shift so that a visible light sensor can
be effectively used.
Preferably said fluid is chosen to be oxygen carrying, such as a blood
substitute, to reduce the risk of hypoxia to the heart muscle.
According to a seventh aspect of the present invention there is provided
a method for reconstructing images by interpolating image data along at least
one of the longitudinal and axial axes of a flexible catheter with a distal end
inserted into a blood vessel and thereby reaching remote places in the
vasculature or other organs, based on image data from both said longitudinal
and axial axes, comprising:
a. off-line image training initialization, and;
b. real-time image data interpolation.
Preferrably said off-line image training initialization comprises:
a. training image construction;
b. reconstruction of a lower resolution new image from said training
image;
c. finding edge directions of said lower resolution image, and; d. training a neural network to obtain a set of filters.
Preferably said training image is clipped and rotated to obtain robust
edges in each one of a plurality of directions.
A preferred embodiment executing local contrast enhancement
following said image data interpolation.
Preferably said local contrast enhancement comprises:
a. calculating the average intensity of said real time image, yielding an
intensity image;
b. generating a first image by correcting the intensity of said intensity
image;
c. calculating a local contrast image;
d. generating a second image by enhancing said local contrast image,
and;
e. summing said first image and said local contrast image to generate
an output image.
Preferably said first image is produced by modifying the intensity of
said real time image using a lookup table.
A preferred embodiment comprises generating said second image by
modifying the local contrast of said real time image using a lookup table.
Preferably said real-time data inteφolation comprises:
a. finding edge directions of each pixel, and;
b. inteφolating data using an appropriate direction filter from a set of
direction filters. A preferred embodiment comprises generating said set of direction
filters in said off-line image training.
BRIEF DESCRIPTION OF THE DRAWINGS
For a better understanding of the invention and to show how the same
may be carried into effect, reference will now be made, purely by way of
example, to the accompanying drawings.
With specific reference now to the drawings in detail, it is stressed that
the particulars shown are by way of example and for puφoses of illustrative
discussion of the preferred embodiments of the present invention only, and are
presented in the cause of providing what is believed to be the most useful and
readily understood description of the principles and conceptual aspects of the
invention. In this regard, no attempt is made to show structural details of the
invention in more detail than is necessary for a fundamental understanding of
the invention, the description taken with the drawings making apparent to those
skilled in the art how the several forms of the invention may be embodied in
practice. In the accompanying drawings:
Fig. 1 is a simplified schematic of the overall patient system.
Fig. 2 A is a simplified schematic of the optical head — side view.
Fig. 2B is a simplified schematic of the optical head — top view.
Fig. 3 is a system block diagram.
Fig. 4A is a simplified schematic of the optical array assembly.
Fig. 4B is a schematic example configuration of optical design A. Fig 4C is a schematic example configuration of optical design B.
Fig. 5A is a simplified diagram of a configuration with the optical head
inside of a transparent balloon distal to a PTCA/stent balloon.
Fig. 5B is a simplified diagram of a configuration with the optical head
adjoining the PTCA/stent balloon.
Fig. 6 is a schematic representation of the image sensor.
Fig. 7 is a block diagram of the post-processing algorithm.
Fig 8 is a simplified schematic of use of an external IR source.
Fig 9 is a simplified schematic of a biological sample collector.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
Before explaining at least one embodiment of the invention in detail, it
is to be understood that the invention is not limited in its application to the
details of construction and the arrangement of the components set forth in the
following description or illustrated in the drawings. The invention is applicable
to other embodiments or of being practiced or carried out in various ways.
Also, it is to be understood that the phraseology and terminology employed
herein is for the puφose of description and should not be regarded as limiting.
The present embodiments preferably provide a diagnostic and operative
system for use in intra-vascular procedures. They consist of the following: 1. A small-diameter flexible catheter, with a distal end that can be
inserted into the blood vessel or any other internal cavity along a guide wire
and reach remote places in the vasculature or other organs; and
2. A viewing apparatus, which is positioned at the distal end of the
catheter, and consists of a specifically designed image sensor, a distorting
optical assembly and an illumination source.
(a) The image sensor is shaped to fit within the restricted dimensions of
the catheter. The image sensor is positioned non-peipendicularly to the
longitudinal axis of the catheter; in a preferred embodiment parallel to the
longitudinal axis of the catheter. The small width of the imaging area makes it
possible to reduce the diameter of the catheter. The design of the sensor allows
the catheter to contain both the viewing apparatus and a working channel
without a prohibitive increase in catheter diameter.
(b) An optical assembly. One preferred embodiment consists of a lens
with two optical planes, a shutter and a prism or mirror with a reflecting
surface. The optical assembly is designed to distort and deflect the light
received from the viewed object to fit the sensor.
(c) The light source or sources may be visible light sources, IR sources
or any combination of the light sources in one embodiment, according to the
embodiment's uses. The lighting is either aimed directly at the imaged object
from the direction of the optical sensor head or directed generally at the scene,
i.e. without directing the light sources straight ahead at the object. 3. One or more working channels, which run along the length of the
catheter, from the proximal end to the distal end, through which therapeutic
instruments can be inserted to the site of their operation. The working channel
is also used for the injection of liquids or gas, as is described in some of the
embodiments. A channel for a guide wire is necessary, and may be provided as
a dedicated channel for the guide wire only or combined with a an injection
channel.
4. A local controller situated at the distal head of the catheter for
coordinating data flow to and from the optical image sensor head and carrying
out commands coming from a central processing and control unit outside the
body regarding, for example, shutter speed and changing the intensity of the
light sources. The communication between the local controller and the central
unit is conducted through a wire connection or a wireless connection. The local
controller may be an entirely separate element situated at the distal head of the
catheter as described above, but it also may be a part of the image sensor.
Another option is that some or all of the local controller's functions are carried
out by the central control and display unit described hereafter.
5. A central control and display unit is typically located on a rack in the
operating/catheterization room. This unit executes, among other tasks, basic
reconstruction of the image including color reconstruction, interface to the user,
display of the video and additional data, manual/automatic control over image
acquisition parameters, and a specific image reconstructing algorithm for improving resolution and local contrasts based on the specific design of the
sensor.
The embodiments described are designed for use in both diagnostic and
therapeutic procedures. Therefore, they can be used on catheters as a viewing
device only or as part of a PTCA, stenting, laser, or any other operative device.
Another option for combining intra-vascular imaging with the diagnostic and
operative devices is by mounting the viewing apparatus at the distal end of a
guide wire. The guide wire is inserted into the artery at the beginning of a
catheterization procedure, and the guide wire guides the catheters used during
the procedure to their proper location. The positioning of the imaging apparatus
on a guide wire makes it possible to use it in very restricted spaces. Positioning
of the imaging apparatus on the guide wire also allows better navigation inside
the vessel and the replacement of the diagnostic and operating tools while
keeping an insertion path open by means of the wire.
Reference is now made to Fig. 1, which is a simplified schematic of the
overall patient-system configuration according to a first preferred embodiment
of the present invention. The configuration has a processing and control unit
28 comprising, among others, three functional units: digital video unit 40;
balloon inflation unit 41; and fluid injection unit 42. The proximal end of the
catheter 30 is connected to the processing and control unit 28. The display unit
50 (typically a monitor) is also connected to the processing and control unit 28.
The catheter 30 is inserted into the patient 25 with the inflatable balloon 31 located at the catheter distal end, inside the patient. A heart rate sensor 26 is
connected to the patient.
The heart rate of the patient 25 is monitored either by a heart rate sensor
26 attached to the patient or by a method described below to determine the
transparency level of the blood. (Such a measurement can indicate blood
pressure changes, and is correlated to heart activity.) Information about the
heart rate is sent to the processing and control unit 28. The processing and
control unit receives the information, processes it and synchronizes the
system's operation with the heart rate. The catheter 30 is connected to the
processing and control unit through three channels: digital video 40, balloon
inflation 41 (for inflating and deflating the inflatable balloon 31 located at the
distal end of the catheter 30, located inside the patient) and fluid injection 42
(used to inject fluids to alter the optical quality of the blood in the immediate
vicinity of the inflatable balloon 31).
Reference is now made to Fig. 2A and 2B which are schematic details of
a side view and a top view, respectively, of the optical head, located on the
distal end of the catheter 30. The optical head comprises a lens 2 and an optical
array, comprising a prism 10, and a sensor array, comprising an illumination
sensor 1 and an image sensor 8 (for acquiring images). The illumination sensor
1 and image sensor 8 may be separate elements or they may be combined
together. One or more illumination sources 3, which may use visible or infrared
or both types of light, are positioned at the distal end of the optical head. A
pressure sensor 7 is also positioned at the distal end of the optical head. A variable volume transparent balloon 6 encloses all components on the distal
end. A mechanical enclosure houses the previously mentioned components and
serves as the proximal surface of the variable volume transparent balloon 6.
Working channel A 4, representing one or more such channels, runs along the
catheter 30 and terminates at the distal end inside of the variable volume
transparent balloon 6. Working channel B 9, representing one or more such
channels, runs along the catheter 30 and terminates distally outside of the
variable volume transparent balloon. A cable 5 runs along the catheter 30 and
connects with the local controller 11 and provides power and communications
for the optical head.
The illumination sources 3 in the present embodiment illuminate the
region immediately in front of the optical head. DC power and electrical signals
are fed to and from the optical head via the cable 5 which is connected at the
distal end to the local controller 11. Working channels (in this example, two)
provide fluid feed and removal and/or other functions inside and outside of the
variable volume transparent balloon 6.
The variable volume transparent balloon 6 enables short period imaging
of a blood vessel (for example) using the visible and/ or infrared illumination
sources 3. The variable volume transparent balloon pressure is sensed and
controlled by the pressure sensor 7 to inflate/ deflate the balloon via air or
liquid provided through working channel A 4. The system has a fixed optical
mechanism comprised of a lens 2 and a prism 10. The variable volume
transparent balloon 6 has known optical attributes and it enables close contact with the blood vessel wall. Inflation of the variable volume transparent balloon
6 enables a clear path for the visible or infrared light directly onto the lens 2.
When deflated, the variable volume transparent balloon 6 allows an
undisturbed flow of blood until the moment before an image is acquired,
whereupon the variable volume transparent balloon 6 is inflated again. At the
time of variable volume transparent balloon 6 inflation, blood flow is
momentarily disturbed to enable a clear view. A safety mechanism, comprising
a pressure sensor 7 ensures that pressure within the balloon is maintained at
acceptable limits. The combination of the pressure sensor 7 and the momentary
pressure supply provide and indication of a possible obstacle in the path of the
catheter. A local controller 11 coordinates data flow to and from the optical
head, as is described in more detail below.
Reference is now made to Figure 3, which is a system block diagram.
Figure 3 highlights the logic in and between the optical head 20, as detailed in
Figures 2A and 2B, with the processing and control unit 28, as described in
Figure 1. The functions of the optical head 20 are grouped logically in Figure
3. The local processor 11 serves to control the functions of the optical head 20
while coordinating signals and power with the processing and control unit 28
located in the operating room. Functions of the optical head 20 are the
illumination source 3 (commanded by the local processor 11), light sensor 8
(which feeds back to the local processor 11), image sensor 1 (which feeds back
to the local processor 11), and shutter 12 (commanded by the local processor
11). The local processor 11 receives and sends commands and receives power from the video control and command unit 40 and power and data control
command unit 13, both of which are located in the processing and control unit
28. The video control and command unit 40 and power and data control
command unit 13 together form the core of command and control of the entire
system. Additional functions are: supply controller 14 (power supply to power
and data control 13), data acquisition and control system 15 (commanded by
power and data control unit 13), and the fluid and air pressure controller 41
(commanded by power and data control unit 13). The fluid and air pressure
controller 41 operates through working channel A 4, which physically passes
through the optical head to enable balloon inflation. In addition, the fluid and
air pressure control 41 commands the physiological fluid control source 42.
The suction mechanism 19 and laser source 18 all function through working
channel B 9, which runs along the catheter but parallel and external to the
optical head. The suction mechanism 19 and laser source 18 are devices that
may be employed in an embodiment described below.
The local processor 11 controls and coordinates functioning of
components previously described on the optical head with the system control
and supply functions located in the operating room. Specific functions of the
power and data control unit 13 include, timing control of the system functions
such as timing of balloon inflation, fluid infusion/injection, activation of light
sources 3, and image sensor 1 activation. The video control and command unit
40 receives digital image infoπnation from the image sensor 1. Corrections of
optical distortion created by the image sensor 1 taking into account the system overall design, are controlled by the video control and command unit 40. Other
functions controlled by the video control and command unit 40 are:
1. Improvement of image resolution based on redundant information
residing in the system, intended specifically for improving image
resolution.
2. Improvement of image quality and image adjustment for the specific
medical application, for example: color, local contrasts, and
emphasis on pathologies.
3. Evaluation of relative temperature based on video information for
spotting pathologic areas suspected as inflamed.
4. Evaluation of the blurring parameters of the image based on the
blurring model of the blood and the acquired image.
5. Reconstruction of the original image according to the blurring model
and evaluated parameters.
Images processed by the video control and command unit 40 may be
displayed, typically on the previously mentioned monitor, as video images in
one of two display modalities. The first modality is a succession of separate
images as received by the image sensor 1. This modality requires a minimal
delay. The second modality is a stream of video images. In order to enable a
stream of video images the processing and control unit 28 performs a time
inteφolation of missing images to provide a continuous image. As a result, a
delay of up to a second between image acquisition and display is typical. Reference is now made to Figure 4 A, which shows a schematic of the
optical array assembly. The optical array assembly 48 is comprised of a lens 2
which is located in front of the shutter 12, which is in turn mounted before the
prism 22. The prism is positioned above the image sensor 1. One preferred
embodiment consists of a lens 2 with two optical planes, a shutter 12 and a
prism 22 or mirror with a reflecting surface. The optical array assembly 48 is
designed to distort and deflect light received from the viewed object to fit the
image sensor 1. The lens 2 and prism 22 are two fixed optical components
whereas the shutter 12 offers flexibility. The shutter 12, as previously
mentioned, is commanded by the processing and control unit, located outside of
the patient at the proximal end of the catheter in the operating room. Schematic
descriptions of two optical design alternatives are depicted on Figs. 4B and 4C.
In Figure 4B PMMA refers to a specific plastic lens material called polymethyl
methacrylate.
Reference is now made to Figure 5A and 5B, which show related
embodiments where a fluid is used to inflate the flexible PTCA or stenting
catheter balloon at the distal end of the catheter. Figure 5 A shows an
embodiment where an optical head 47 is located distally to the PTCA/stent
balloon 50. The stent balloon 50 is located distally to the catheter 30. The
optical head 47 is located within a second balloon 60. A regulating valve 55 is
located between the PTCA/stent balloon 50 and the second balloon 60.
Inflation of the second balloon 60 is enabled by the regulating valve 55, which
allows the second balloon 60 to be initially inflated, followed by inflation of the stent balloon 50. Note that the optical head shown in Figure 5A is similar to
the optical head previously shown in Figure 2, in that the functions of on-board
multiple light sources, on board light receivers, and an on board pressure sensor
are preferably included. The regulating valve 55 is designed to close itself
under high pressure and enables the inflation of the PTCA/stent balloon 50.
Once the second balloon 60 is inflated and the pressure inside is high enough,
the valve closes and the PTCA/stent balloon 50 inflates. The injected fluid
inflates the second balloon 60, made of a transparent membrane which is non-
permeable to red blood cells, to remove the red blood cells from the field of
view and reduce the scattering of light. The optical characteristics of the
injection fluid are discussed hereafter. The regulating valve 55 also controls
deflation of both the PTCA/stent balloon 50 and the second balloon 60.
Figure 5B shows an embodiment where the optical head 48 is installed
distally and exterior to the PTCA/stent balloon 50. The optical head assembly
48 is mounted on the fluid injection channel 75, which terminates in a
regulating valve 56, located at the distal end of the fluid injection channel 75.
The PTCA/stent balloon 50 is located at the distal end of the catheter. Note
that the optical head assembly 48 shown in Figure 5B is similar to the optical
head previously shown in Figure 2 in that the functions of on-board multiple
light sources and on board light receiver are preferably included. In the present
embodiment, a regulating valve 56 located distally to the PTCA/stent balloon
50 controls the flow of injected fluid distally outside of the PTCA/stent balloon 50 to momentarily clear the field of view in front of the optical assembly and
allow images to be acquired.
The embodiments shown in Figures 5A and 5B operate in a cyclical
manner. Every heartbeat sensed by the previously mentioned heart rate sensor,
initiates a new device cycle. Each cycle comprises a delay after which fluid is
injected in order to inflate the second balloon 60 as in figure 5 A or clear the
field of view as in figure 5B. Inflation of the second balloon 60 and fluid
injection are synchronized and timed so that they occur after a pulse of blood
which is pushed from the heart. The regulating valve 56 is opened and fluid is
infused into the artery to improve the visibility at the distal end of the catheter.
A short period after the start of fluid infusion, the optical head assembly 48
starts acquiring images of the scene. The previously-mentioned light sources
are powered in synchronized pulses with the frame rate of the optical head
assembly 48 to increase the ratio between the effective light absorbed by the
optical head assembly 48 and power dissipation of the light source. After
obtaining several images and in synchronization with the beginning of the next
heart beat, the system stops both image acquisition and infusion of fluid and
reduces the pressure inside the second balloon 60.
The embodiments shown in Figures 5 A and 5B are not space-consuming
because one channel is used for inflating both balloons (Figure 5A) or for
inflating and injecting fluid into the blood vessel (Figure 5B), thus allowing a
smaller width catheter. Reference is now made to Figure 6, which is a simplified diagram
showing an image sensor 70. The sensor comprises an imaging area 71 which
is shaped as a rectangle pixel area, such as a 128 x 256 pixel array. The sensor
may also contain additional circuitiy 72 that performs functions such as analog
to digital conversion, timing control, and local control. I/O. Supply pads 73 are
indicated. The sensor 70 is located in the optical head assembly previously
noted in Figures 2, 3, and 4A, 4B, and 4C. The sensor 70 serves to capture the
visible or IR light from the scene as shaped by the lenses and shutters located in
front of it. As previously noted, the sensor is positioned non-peφendicularly to
the longitudinal axis of the catheter. In a preferred embodiment it is placed
parallel to that axis. The small width of the imaging area makes it possible to
reduce the diameter of the catheter.
Reference is now made to Figure 7. Figure 7 is a simplified block
diagram describing a post-processing algorithm, which reconstructs the
displayed image based on a training sequence and a real time image, once an
image has been received by the central control and display unit. The central
control and display unit is preferably located in the operating room, and it
receives images from the image sensor, preferably located at the distal end of
the catheter, preferably located in a blood vessel.
The initialization and training sequence 301 takes place as a one-time
off-line process. The aim of this sequence is to determine the optimal set of
filters for reconstructing the real-time image. The sequence begins by
construction of a training image, followed by clipping and rotating the image to obtain robust edges in all directions 302. For illustration puφoses the training
image size may be N by N pixels. Then, pre input image conversion 303 takes
place involving construction of a new image from the training frame in order to
obtain an input to a neural network. The input image size selected for this case
is N/2 by N pixels, but the algorithm works with other image sizes. Input image
conversion 303 is then performed by finding the edge direction 304 at each
pixel of the input according to neighborhood decision vote, followed by
training the neural network 305 to obtain a set of filters. The training process is
performed on the intensity image (a black and white gray level image). The
result at this point is a set of filters (weights) to be used on the real-time
sequence.
Real-time execution begins with step 306, when a new image is received
307. If there are no more images, execution is completed 317. If a new image is
received, the next step is to find the direction for each pixel 308 in the intensity
input image according to the neighborhood decision vote. The neural networks'
filters are then run 309, in accordance with the directions for each color plane,
which is performed separately. If contrast enhancement is necessary 310, a
series of steps are performed, as noted below. If contrast enhancement is not
necessary, a new image is received 307.
The first step of contrast enhancement is to perform image segmentation
311 based on local average intensity. The following steps are performed:
calculate average intensity 312, taking into account only neighbors with
relatively close values, and; correct average intensity 313 using look up tables (LUT) which optimizes the dynamic range of the system (camera and display
device). In parallel to the two previous steps, the following are performed:
calculate local image contrast 314 and; enhance local contrast 315. The
enhancement function is a function of the average intensity and the local
contrast and it is done by means of LUT. Generation of the final image 316
utilizes the previous steps of contrast and intensity enhancement, summing the
local contrast and the average intensity. At this point, a new image is received
307. This logic continues until there are no new images and the algorithm ends
317.
Methods for Imaging in the Presence of Opaque Liquids
The following are various preferred embodiments for different methods
and applications designed to achieve visibility through a medium of an opaque
liquid, preferably, in blood. It is important to emphasize that the various
embodiments described below can be used either separately as stand-alone
systems or in any combination with each other.
1. Lighting with Near-IR wavelengths:
There are three properties of light that effect the visibility of light with a
specific wavelength passing through a medium: scattering, absoφtion, and
attenuation. Scattering is significant in both near-IR and visible light when
passing through blood. Absoφtion and attenuation, on the other hand, are
minimal in near-IR radiation. Therefore, near-IR light may be advantageous
when compared to visible light for effective illumination through such a
medium as blood. In the following text, it should be noted that wherever IR is mentioned, near-IR (radiation with wavelengths shorter than 1 μm) is preferably
used, unless specified otherwise.
The fact that IR light absoφtion is minimal in a blood medium means
that IR light may be used in a viewing apparatus designed for intra-vascular
imaging in combination with other methods mentioned in the present
disclosure. The apparatus and method in the present embodiment includes a
flexible catheter with a viewing apparatus at its distal end, a working channel
running from the proximal to the distal end, and a local controller at the distal
end. The previously mentioned imaging sensing apparatus is applicable to the
present embodiment. The apparatus consists of one or more light sources which
emit IR light, an image sensor that is able to receive this light, and an optical
assembly. The image sensor is preferably a CMOS or CCD pixilated sensor. In
order to allow acquisition of IR images, the sensor may use filters that have
band passes at IR wavelengths. Silicon-based devices (CMOS, CCD) exhibit a
reasonably good response to IR wavelengths of up to lμm.
The light sources may also include a combination of wavelengths of
visible and IR light, requiring appropriate sensors to receive multiple light
wavelengths. Illuminating the scene with multiple wavelength light sources
enables acquisition of several types of pictures for diagnostic puφoses.
IR light can be used in another diagnostic embodiment, considering the
fact that in general, different human tissues and different substances have
different absoφtion, scattering, and attenuation coefficients in the IR region.
The present embodiments can include an analyzing apparatus for the analysis of these coefficients. Evaluation of blood status (for example, sugar level in the
blood may be analyzed by evaluating the IR light absorption) may be one of the
applications of the present embodiment. Several pathologies in the vessel tissue
may be analyzed in the same way.
Another embodiment uses external IR illumination. Reference is made to
Figure 8. The optical assembly 80 is located at the distal end of the catheter 30
within the patient's body 85, preferably in a blood vessel. An exterior IR light
source 88 exterior to the patient's body illuminates the field of view in front of
the optical assembly. Note that the optical head assembly 80 shown in Figure 8
is similar to the optical head assembly 80 previously shown in Figure 2 in that
the function of on- light receiver is preferably included. However, in the
present embodiment, the light source is not on board the optical head assembly
80, rather it is exterior to the patient.
2. Changing the optical properties of blood
Another method and embodiment make use of light sources utilizing
visible light or IR radiation. Blood is opaque in visible light illumination
because blood contains suspended cells. This phenomenon is much like that
encountered with water vapor drops in fog; even though the content of the red
blood cells is transparent, when the content of red blood cells is arranged in
"drops" surrounded by a membrane, the reflectance factor of the solution yields
an opaque situation. Therefore, in order to obtain a clear vision of the field of
view, blood may be temporarily diluted at the site of an object to be imaged. The injection fluid is not necessarily a physiological fluid. One possible
embodiment uses a fluid with a reflectance factor identical or similar to the
reflectance factor of red blood cells, or a fluid that creates such a reflectance
factor when mixed in a certain concentration with blood. This type of fluid
solves the problem of light scattering in blood, leaving only a light absoφtion
problem, which is much simpler to solve. The present embodiment includes a
flexible catheter, a viewing apparatus and a local controller at the distal end and
a working channel, through which the fluid may be injected from the proximal
end into the blood vessel or injected directly into the vessel. Another option is
to inject the fluid through the guide wire channel. The amount of injected fluid
is controlled centrally by a processing device, and is determined according to
the transparency level of the blood, measured by the reflection of illumination
from the light source onto the light sensor as previously described, or according
to a sensor connected to the patient outside of the patient's body. Such a light
measurement may supply the timing to inject the physiological fluid into the
vessel. In another application, the reflected light measurement may provide for
analysis of blood pressure changes by measuring the amplitude of the light
reflected into the sensor, according to the level of heart activity. There is a
correlation between the amplitude of light received by the sensor and blood
pressure.
Variations in the amount and timing of fluid injection may be determined
by a quality control algorithm, which may be able to calculate necessary changes to lighting or fluid injection from the received image to improve image
quality.
A further embodiment of the present invention uses either a fluid with a
physiological concentration of particles or a fluid with less than a physiological
concentration of particles, such as 1/6 saline. The latter type of fluid can cause
hemolysis of some of the red blood cells, thus improving the reflectance factor
of the liquid, and reducing the above-mentioned phenomenon of light scattering
in blood. Another embodiment uses a fluid that is capable of carrying oxygen,
such as a blood substitute, thus reducing the risk of hypoxia to the heart
muscle; this compared to injecting a fluid not capable of carrying oxygen to
body tissues into the artery.
Yet another embodiment uses a fluid that enables a frequency conversion
of light, i.e. from IR wavelengths to the visible light spectrum, thus making it
possible to use a visible light optical sensor and nevertheless retaining the
advantages of illuminating with IR light.
3. Transparent structure at the distal end
The present embodiment also makes use of light sources in the visible
light or IR wavelengths. There is a need to displace the blood in order to clear
the field of view. This embodiment uses a transparent dome or balloon, either
rigid or flexible. The structure is positioned at the distal end of the catheter,
beyond the viewing apparatus. In one form of the embodiment previously
described and referred to in Figures 5A and 5B, the structure at the distal end is
a flexible balloon, which inflates by injecting a transparent fluid or gas into it. It is positioned at the distal end of the catheter at its deflated mode. The
injection is preferably, centrally controlled and the fluid or gas may be injected
to inflate the balloon whenever the viewing apparatus is activated. When
inflated, the balloon displaces the blood from the field of view, as does the
dome described above. In another form of the embodiment, the structure is a
rigid dome, which is positioned around and at the edge of the distal end and
extends distally to it. The rigid structure is situated so that it removes the blood
from around the viewing apparatus, thus" "clearing the field of view between the
dome and the apparatus without blocking the flow of blood in the artery. The
rigid structure is either hollow (vacuum, gas) or filled with a transparent fluid.
4. Polarized light filter
Light that impinges on a surface has a component that returns polarized.
Reflected light is more polarized when the incidence angle is closer to normal.
In an intra-vascular surrounding, light hitting the wall and/or any structures
connected to it returns mostly polarized, while the light hitting suspended cells
in the fluid filling the vessel does not return polarized. Imaged objects are
usually surfaces connected to the vessel's wall. As a result, by situating a
polarized light filter before the optical assembly, light reaching the sensor may
be only polarized light, i.e. the light reflected from the imaged structure. This
method of using polarized light increases the image/noise ratio and improves
the quality of the received image.
Other Possible System Embodiments In addition to the embodiments previously discussed, the following represent
four other possible embodiments, related to previously described embodiments:
1. An optical sensor head with two sensors for obtaining a stereoscopic
image.
2. A distal balloon made of a transparent membrane blocking the
passage of red blood cells but allowing the passage of fluids. In the
present embodiment, the injected fluid can also be used for the
inflation of the distal balloon membrane.
3. Laser operated surgery mechanism using service channel and local
imaging device(s). This embodiment enables an accurate operation
procedure with continuous imaging of the operation area.
4. Mounting the viewing apparatus close to the front end of a needle
for performing biopsies and other diagnostic or therapeutic
procedures.
5. Another embodiment is that of biopsy and sample retrieval.
Reference is made to Figure 9. Working channel B 9 is used to pass
either or both the suction and nano-gripper 9$ and the laser device
98 distally, in front of the optical head 90. Biological sample
collection, using a suction/nano-gripper 99 mechanism and the
optical head 90 to enable visual inspection of the desired location.
Samples may be transferred through the working channel B 9
outside the patient's body for analysis. The suction/nano-gripper 99
is used to hold a sample in position and the laser apparatus is used to cut the sample from surrounding tissue. The optical head 90 is
similar to the previously mentioned optical head configuration. The
suction/nano-gripper 99 and laser device 98 can alternately or
together be positioned in front of the optical head 90 to provide
visual feedback. This process enables biopsy of samples which can
be removed from the patient's body through working channel B 9.
The application in the field^ of cardiovascular therapy is only one of the
possible applications for the present invention. Minimally invasive surgery is
applied in many fields of medical diagnosis and therapy, such as in other
vascular, breast, urethral and renal, and abdominal procedures, for example,
and the present invention may be applied in these fields.
It is appreciated that certain features of the invention, which are, for
clarity, described in the context of separate embodiments, may also be provided
in combination in a single embodiment. Conversely, various features of the
invention which are, for brevity, described in the context of a single
embodiment, may also be provided separately or in any suitable sub
combination.
It will be appreciated by persons skilled in the art that the present
invention is not limited to what has been particularly shown and described
hereinabove. Rather the scope of the present invention is defined by the
appended claims and 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.

Claims

1. An invasive imaging apparatus comprising:
a. A flexible catheter with a proximal end and a distal end, said
distal end being shaped for insertion into a blood vessel along a guide wire
thereby to reach remote places in the vasculature or other organs.
b. An optical assembly positioned at the distal end of said catheter
comprising an image sensor positioned non-peφendicularly to the longitudinal
axis of said catheter.
c. At least one illumination source for illuminating an immediate
region beyond the distal end of said catheter.
d. At least one working channel running from the proximal to the
distal end of said catheter.
2. Apparatus according to claim 1 wherein said illumination source
utilizes at least one wavelength taken from within a range comprising visible
light, near infra-red, and infra-red light.
3. Apparatus according to claim 2 comprising a plurality of
illumination sources and wherein said illumination sources are controlled
together.
4. Apparatus according to claim 2, comprising a plurality of
illumination sources and wherein said illumination sources are controlled
separately.
5. Apparatus according to claim 1 wherein said illumination source
uses at least one wavelength preselected to improve visibility through blood.
6. Apparatus according to claim 1 wherein said illumination source
is comprised of an infra-red illumination source positionable outside of said
patient's body.
7. Apparatus according to claim 4 wherein said illumination source
is controllable to be aimed directly at an imaged object from the direction of
said imaging assembly.
8. Apparatus according to claim 1, wherein said illumination source
is controllable to be directed in a general viewing direction.
9. Apparatus according to claim 1 wherein said optical assembly
comprises optical components and an imaging assembly.
10. Apparatus according to claim 9 wherein said imaging assembly
comprises said image sensor and an illumination sensor.
1 1. Apparatus according to claim 9 wherein said optical components
comprise a lens with two optical planes, a shutter, and a light deflector.
12. Apparatus according to claim 11 wherein said light deflector is
one of a prism and a mirror with a reflecting surface.
13t Apparatus according to claim 10 wherein said image sensor and
said illumination sensor are operable to sense at least one wavelength taken
from within a range from visible light to infra-red light to correspond to said
illumination source.
14. Apparatus according to claim 10 wherein a polarized filter is
positionable before at least one of a member of a group comprising said
illumination sensor, said image sensor, said illumination sources, and said lens,
and wherein said polarized filter polarization direction is controllable to
enhance image quality.
15. Apparatus according to claim 1 comprising a central control and
display unit connectable to the proximal end of said catheter from outside of
the patient's body.
16. Apparatus according to claim 1 wherein said working channel
comprises a guide wire.
17. Apparatus according to claim 1 wherein said working channel is
usable for controllably passing through fluid to said distal end of catheter.
18. Apparatus according to claim 10 wherein said image sensor is
positioned substantially parallel to the longitudinal axis of said catheter.
19. Apparatus according to claim 10 wherein said image sensor is
shaped to fit within restricted dimensions of said catheter.
20. Apparatus according to claim 10 wherein said image sensor is a
CMOS or CCD-based pixel sensor.
21. Apparatus according to claim 10 wherein said image sensor
comprises an imaging area shaped in a rectangular pixel array.
22. Apparatus according to claim 21 wherein said rectangular pixel
array measures 128 x 256 pixels.
23. Apparatus according to claim 10 wherein said sensor comprises
sensor control electronic circuitry located beneath a shorter side of said
imaging area, said imaging area being arranged as a rectangular pixel array.
24. Apparatus according to claim 23 wherein I/O and supply pads for
said electronic circuitry are placed along at least one of the shorter sides of said
image sensor.
25. Apparatus according to claim 1 further comprising a local
controller located at the distal end of said catheter to coordinate data flow to
and from said optical assembly and to perform commands received from said
central control and display unit.
26. Apparatus according to claim 17 wherein said display and control
unit is operable to control the timing and amount of injection of said fluid.
27. Apparatus according to claim 1 wherein a transparent balloon¬
like structure is positioned at said distal end of said catheter to displace blood
from around the optical sensor-head, allowing clear visibility.
28. Apparatus according to claim 27 wherein said balloon-like
structure is rigid.
29. Apparatus according to claim 27 wherein said balloon-like
structure is flexible.
30. Apparatus according to claim 29 wherein said balloon-like
structure is inflated and deflated by means of using a liquid or a gas passed
through said working channel.
31. Apparatus according to claim 1 wherein said optical assembly
comprises two image sensors for obtaining a stereoscopic image.
32. An apparatus according to claim 30 wherein the injection of said
fluid is synchronized with the operation of said optical assembly, synchronizing
said operation and said injection with the cycle of patient physiological
conditions.
33. Apparatus according to claim 32 wherein one of said
physiological conditions is heart beat sensible using a heart rate sensor
connectable to a patient's body from outside of said patient's body or insertable
into said blood vessel through said catheter.
34. Apparatus according to claim 33, wherein said heart rate sensor
comprises a plethysmograph.
35. Apparatus according to claim 33 wherein information from said
heart rate sensor is transferred to said central control unit enabling
synchronization with said physiological conditions.
36. Apparatus according to claim 30 wherein said balloon-like
structure is pressure-sensed to provide real-time feedback when said balloon¬
like structure impinges upon an obstacle, such as a blood vessel wall.
37. Apparatus according to claim 1 wherein said working channel is
usable for passage of therapeutic instruments to a site of operation.
38. Apparatus according to claim 1 wherein said optical assembly is
used in conjunction with a laser cutting device to enable laser operated surgery.
39. Apparatus according to claim 1 wherein said laser cutting device
is used to obtain biopsy biological samples by cutting and transferring through
said working channel to the proximal end of said catheter.
40. Apparatus according to claim 39 wherein said optical assembly
and said laser cutting device are used in conjunction with one of a suction and
nano-gripper mechanisms to enable visual inspection of a desired location for
biological sample retrieval.
41. A method for performing biopsies and other diagnostic or
therapeutic procedures comprising placing an invasive optical assembly
apparatus on the distal end of a needle, inserting said optical assembly and
needle into vasculature or other organs, and using said optical assembly to
provide visual feedback of said biopsies and diagnostic or therapeutic
procedures.
42. A method for viewing through blood in Situ comprising injecting
a controlled amount of fluid into blood in the immediate region in front of an
invasive optical assembly, temporarily changing the optical characteristics of
the blood in said immediate region, and thereby improving visibility through
said blood.
43. A method for viewing through blood in Situ comprising injecting
a controlled amount of fluid into blood in the immediate region in front of an
invasive optical assembly, temporarily changing the reflectance of the liquid
portion of said blood, and improving visibility through said blood.
44. A method for viewing through blood in Situ according claim 42
wherein said fluid is used to change the optical characteristics of blood in Situ
to facilitate imaging through said blood, said fluid being a physiological fluid,
such as saline, or a hypoosmolar fluid, such as 0.45% saline or 1/6 saline.
45. A method for viewing through blood in Situ according to claim
42 wherein said fluid for use in changing the optical properties of blood in Situ
to facilitate imaging through said blood, said fluid being a blood substitute
which does not contain red blood cells and has homogenous optical
characteristics.
46. A method for viewing through blood in Situ according to claim
42 wherein said fluid is chosen to enable illumination to facilitate imaging
through said blood and the environment in Situ with an IR illumination source,
enabling a frequency shift so that a visible light sensor can be effectively used.
47. A method for viewing through blood in Situ according to claim
42 wherein said fluid is chosen to be oxygen carrying, such as a blood
substitute, to reduce the risk of hypoxia to the heart muscle.
48. An invasive imaging control apparatus comprising:
a. A flexible catheter with a proximal end and a distal end, said distal
end being shaped for insertion into a blood vessel along a guide wire thereby to
reach remote places in the vasculature or other organs.
b. An optical assembly positioned at the distal end of said catheter.
c. At least one working channel running from the proximal to the distal
end of said catheter. d. A control unit for regulating the opacity level of blood in said blood
vessel around said distal end of said catheter, controllably injecting quantities
of fluid into said blood vessel in the vicinity of said optical assembly, thereby
enhancing visibility.
49. Apparatus according to claim 48 wherein said optical assembly
comprises an illumination sensor operable to sense at least one wavelength
taken from within a range from visible light to infra-red light.
50. Apparatus according to claim 48 wherein said working channel is
usable for controllably passing through fluid to said distal end of catheter.
51. Apparatus according to claim 48 wherein said control unit is
connectable to the proximal end of said catheter from outside of the patient's
body.
52. Apparatus according to claim 48 wherein said control unit is
operable to control the timing and amount of injection of said fluid.
53. Apparatus according to claim 52 wherein the injection of said
fluid is synchronized with the operation of said optical assembly, synchronizing
said operation and said injection with the cycle of patient physiological
conditions.
54. Apparatus according to claim 48 wherein said fluid is insertable
into the immediate region of said distal end of said catheter to change the
optical characteristics of blood in said immediate region.
55. Apparatus according to claim 48 wherein said fluid comprises
one or more fluids selected to modify the optical characteristics of blood
plasma to render said optical characteristics to be as close as possible to those
of red blood cells.
56. Apparatus according to claim 53 wherein said physiological
condition is heart beat sensible using a heart rate sensor connectable to a
patient's body from outside of said patient's body or insertable into said blood
vessel through said catheter.
57. Aparatus according to claim 56, wherein said heart rate
sensor comprises a plethysmograph.
58. Apparatus according to claim 56 wherein information from said
heart rate sensor is transferred to said central control unit enabling
synchronization with said physiological conditions.
59. An invasive imaging control apparatus comprising: a. A flexible catheter with a proximal end and a distal end, said distal
end being shaped for insertion into a blood vessel along a guide wire thereby to
reach remote places in the vasculature or other organs.
b. An optical assembly positioned at the distal end of said catheter.
c. At least one working channel running from the proximal to the distal
end of said catheter
d. A semi-permeable membrane positioned at said distal end of said
catheter, surrounding said optical assembly extendable to displace blood from
around the optical assembly allowing clear visibility.
60. Apparatus according to claim 59 wherein said membrane is rigid.
61. Apparatus according to claim 59 wherein said membrane is
flexible.
62. Apparatus according to claim 59 wherein said membrane is
inflated and deflated by means of controllably passing a fluid through said
working channel to said distal end of catheter.
63. Apparatus according to claim 59 comprising a control unit
connectable to the proximal end of said catheter from outside of the patient's
body.
64. An apparatus according to claim 62 wherein the injection of said
fluid is synchronized with the operation of said optical assembly, synchronizing
said operation and said injection with the cycle of patient physiological
conditions.
65. Apparatus according to claim 64 wherein one of said
physiological conditions is heart beat sensible using a heart rate sensor
connectable to a patient's body from outside of said patient's body or insertable
into said blood vessel through said catheter.
66. Apparatus according to claim 65 wherein information from said
heart rate sensor is transferred to said central control unit enabling
synchronization with said physiological conditions.
67. A method for reconstructing images by inteφolating image data
along at least one of the longitudinal and axial axes of a flexible catheter with a
distal end inserted into a blood vessel and thereby reaching remote places in the
vasculature or other organs, based on image data from both said longitudinal
and axial axes, comprising:
a. off-line image training initialization, and;
b. real-time image data inteφolation.
68. A method of reconstructing images according to claim 67
wherein said off-line image training initialization comprises:
a. training image construction;
b. reconstruction of a lower resolution new image from said training
image;
c. finding edge directions of said lower resolution image, and;
d. training a neural network to obtain a set of filters.
69. A method of reconstructing images according to claim 68
wherein said training image is clipped and rotated to obtain robust edges in
each one of a plurality of directions.
70. A method of reconstructing images according to claim 67
comprising executing local contrast enhancement following said image data
inteφolation.
71. A method according to claim 70 wherein said local contrast
enhancement comprises:
a. calculating the average intensity of said real time image, yielding an
intensity image;
b. generating a first image by correcting the intensity of said intensity
image;
c. calculating a local contrast image; d. generating a second image by enhancing said local contrast image,
and;
e. summing said first image and said local contrast image to generate
an output image.
72. A method according to claim 71 comprising generating said first
image by modifying the intensity of said real time image using a lookup table.
73. A method according to claim 71 comprising generating said
second image by modifying the local contrast of said real time image using a
lookup table.
74. A method according to claim 67 wherein said real-time data
inteφolation comprises:
a. finding edge directions of each pixel, and;
b. inteφolating data using an appropriate direction filter from a set of
direction filters.
75. A method according to claim 74 comprising generating said set
of direction filters in said off-line image training.
PCT/IL2002/000659 2001-08-10 2002-08-11 Intra vascular imaging method and apparatus WO2003013624A2 (en)

Priority Applications (6)

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US20040147806A1 (en) 2004-07-29
US20020068853A1 (en) 2002-06-06
AU2002324316A1 (en) 2003-02-24
US20070100241A1 (en) 2007-05-03
JP4471651B2 (en) 2010-06-02
EP1465684A4 (en) 2009-01-07
JP2005503203A (en) 2005-02-03
US7758499B2 (en) 2010-07-20
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EP1465684A2 (en) 2004-10-13
CA2456418A1 (en) 2003-02-20

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