US20150305604A1 - System and method for visualizing tissue with an icg dye composition during ablation procedures - Google Patents
System and method for visualizing tissue with an icg dye composition during ablation procedures Download PDFInfo
- Publication number
- US20150305604A1 US20150305604A1 US14/697,065 US201514697065A US2015305604A1 US 20150305604 A1 US20150305604 A1 US 20150305604A1 US 201514697065 A US201514697065 A US 201514697065A US 2015305604 A1 US2015305604 A1 US 2015305604A1
- Authority
- US
- United States
- Prior art keywords
- tissue
- lesion
- icg
- energy
- surgical site
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- BDBMLMBYCXNVMC-UHFFFAOYSA-N CC1(C)C2=C(C=CC3=CC=CC=C32)[N+](CCCCS(=O)(=O)O)=C1/C=C/C=C/C=C/C=C1\N(CCCCS(=O)(=O)[O-])C2=C(C3=C(C=CC=C3)C=C2)C1(C)C.[Na+] Chemical compound CC1(C)C2=C(C=CC3=CC=CC=C32)[N+](CCCCS(=O)(=O)O)=C1/C=C/C=C/C=C/C=C1\N(CCCCS(=O)(=O)[O-])C2=C(C3=C(C=CC=C3)C=C2)C1(C)C.[Na+] BDBMLMBYCXNVMC-UHFFFAOYSA-N 0.000 description 1
- 0 CC1(C)c(c(cccc2)c2cc2)c2*(CCCCS(O)(=O)=O)=C1C=CC=CC=CC=C(C1(C)C)N(CCCCS([*+])(=O)=O)c2c1c(cccc1)c1cc2 Chemical compound CC1(C)c(c(cccc2)c2cc2)c2*(CCCCS(O)(=O)=O)=C1C=CC=CC=CC=C(C1(C)C)N(CCCCS([*+])(=O)=O)c2c1c(cccc1)c1cc2 0.000 description 1
Images
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
- A61B1/04—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
- A61B1/043—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 for fluorescence imaging
-
- 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
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B18/1492—Probes or electrodes therefor having a flexible, catheter-like structure, e.g. for heart ablation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/18—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves
- A61B18/20—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/0033—Features or image-related aspects of imaging apparatus classified in A61B5/00, e.g. for MRI, optical tomography or impedance tomography apparatus; arrangements of imaging apparatus in a room
- A61B5/0036—Features or image-related aspects of imaging apparatus classified in A61B5/00, e.g. for MRI, optical tomography or impedance tomography apparatus; arrangements of imaging apparatus in a room including treatment, e.g., using an implantable medical device, ablating, ventilating
-
- 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
- A61B5/0071—Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence by measuring fluorescence emission
-
- 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
- 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
- A61B1/00002—Operational features of endoscopes
- A61B1/00043—Operational features of endoscopes provided with output arrangements
- A61B1/00045—Display arrangement
- A61B1/0005—Display arrangement combining images e.g. side-by-side, superimposed or tiled
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00017—Electrical control of surgical instruments
- A61B2017/00022—Sensing or detecting at the treatment site
- A61B2017/00057—Light
- A61B2017/00061—Light spectrum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00571—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body for achieving a particular surgical effect
- A61B2018/00577—Ablation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00982—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body combined with or comprising means for visual or photographic inspections inside the body, e.g. endoscopes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/36—Image-producing devices or illumination devices not otherwise provided for
- A61B90/37—Surgical systems with images on a monitor during operation
- A61B2090/373—Surgical systems with images on a monitor during operation using light, e.g. by using optical scanners
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/36—Image-producing devices or illumination devices not otherwise provided for
- A61B90/37—Surgical systems with images on a monitor during operation
- A61B2090/376—Surgical systems with images on a monitor during operation using X-rays, e.g. fluoroscopy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/39—Markers, e.g. radio-opaque or breast lesions markers
- A61B2090/3937—Visible markers
- A61B2090/3941—Photoluminescent markers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/30—Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/36—Image-producing devices or illumination devices not otherwise provided for
- A61B90/361—Image-producing devices, e.g. surgical cameras
Definitions
- the present disclosure relates to ablation instruments and methods of use thereof, in particular to ablation catheters and methods for visualizing tissue using an ICG dye composition to identify and distinguish ablative tissue from de novo tissue.
- Cardiac arrhythmias are irregularities in the normal beating pattern of the heart and can manifest themselves in either the atria or the ventricles of the heart.
- atrial fibrillation is a form of arrhythmia characterized by rapid randomized contractions of atrial myocardium, causing an irregular, often rapid ventricular rate.
- the regular pumping function of the atria is replaced by a disorganized, ineffective quivering as a result of chaotic conduction of electrical signals through the upper chambers of the heart.
- Atrial fibrillation is often associated with other forms of cardiovascular disease, including congestive heart failure, rheumatic heart disease, coronary artery disease, left ventricular hypertrophy, cardiomyopathy, or hypertension.
- Atrial fibrillation paroxysmal and persistent
- ectopic foci tissue that are located in one or more of the four pulmonary veins, which attach to the rear of the left atrium. It has been found that atrial fibrillation may be cured by electrically isolating the pulmonary veins from the rest of the atrium.
- circumferential ablation of tissue at the junction of the pulmonary veins and the left atrium has been practiced to treat atrial fibrillation.
- electrical conductivity from one segment to another can be blocked and the resulting segments become too small to sustain the fibrillatory process on their own.
- ablation devices have recently been proposed for creating lesions to treat cardiac arrhythmias.
- Many of the recently proposed ablation instruments are percutaneous devices that are designed to create such lesions from within the heart.
- Such devices are positioned in the heart by catheterization of the patient, e.g., by passing the ablation instrument into the heart via a blood vessel, such as the femoral vein.
- percutaneous devices are positioned with the assistance of a guide catheter and guide wire, which are first advanced into heart.
- a guide catheter or similar guide device is advanced through the vasculature and into the left atrium of the heart.
- a guide wire is then advanced toward a pulmonary vein.
- a catheter instrument with an expandable element is then advanced through the guide catheter and over the guide wire and into the pulmonary vein where the expandable element (e.g., a balloon) is inflated.
- the balloon includes a circumferential ablation element, e.g., an energy emitting device, such as a laser, disposed in the inner surface of the balloon, which performs the ablation procedure.
- ablation near or within the pulmonary vein can result in complications. Overtreatment deep within a vein can result in stenosis (closure of the vein itself), necrosis or other structural damage, any of which can necessitate immediate open chest surgery. Conversely, undertreatment in which scar tissue formed is not continuous and/or insufficient to replace the cardiac muscles sought to be electrically isolated from the atrium will cause the surgical ablation procedure to be unsuccessful. Thus, repeating of the surgical ablation procedure is then required which is almost always undesirable.
- the lesions are not visible for various reasons.
- the ablation energy in these procedures typically penetrates deeply into the atrial tissue to create the lesion while leaving the endocardial surface relatively undamaged.
- color video cameras are often not sensitive enough to discriminate the subtle color changes that distinguish treated and untreated tissue.
- the light levels delivered to the site are limited since they typically travel to the treatment site via a small optical fiber thereby further hindering the ability of video cameras to visualize these distinctions.
- the present invention is directed to the use of an indocyanine green (ICG dye) composition as part of an imaging system for distinguishing lesions from de novo tissue.
- a tissue ablation system for identification of a lesion formed by directed energy emission at a surgical site of a patient includes a source of an indocyanine green (ICG dye) composition for delivery into a body of the patient including to the surgical site.
- the system further includes a tissue ablation instrument for use at the surgical site.
- the instrument includes a movable directed first energy emitter configured to emit a variable amount of directed energy for ablating tissue and forming a lesion at the surgical site.
- a second energy emitter is provided for applying energy of a type and in an amount sufficient to cause the ICG composition to fluoresce.
- the system further includes an imaging device that is configured to obtain an image of the surgical site while the ICG fluoresces with the lesion being visually identifiable relative to de-novo tissue based on a lack of observable fluorescence at locations of the lesion, while the de-novo tissue is characterized by areas of fluorescence.
- a display such as a computer monitor, displays the image in real time.
- the formed lesion is immediately and readily visually distinguishable from the de novo tissue and blood due to the bright fluorescence of the de novo tissue and blood versus the formed lesion being characterized by a lack of fluorescence, the user (surgeon) can detect deficiencies in the lesion, such as gaps or breaks in the lesion, and take immediate corrective measures.
- FIG. 1 is a block diagram depicting the components of an endoscope-guided cardiac ablation system according to the invention
- FIG. 2 is a schematic view of the of the cardiac ablation instrument of the cardiac ablation system of FIG. 1 ;
- FIG. 3 is a block diagram of the processor modules used in the cardiac ablation instrument.
- FIG. 4 illustrates a user interface in the form of a splint-screen arrangement for displaying information
- FIG. 5 is a schematic view of the cardiac ablation instrument of FIG. 2 shown in a treatment position at a surgical site in the pulmonary vein;
- FIG. 6 is a schematic view of the cardiac ablation instrument of FIG. 2 with its compliant balloon inflated and its ablation element deployed at one of a plurality of locations;
- FIG. 7 is a flow diagram illustrating the steps performed by the ablator system of FIG. 1 for determining the quality of lesions formed during a surgical ablation procedure;
- FIG. 8 is a screen shot of the display of FIG. 1 depicting visual warning signals indicative of insufficient lesions
- FIG. 9 is a block diagram of a computer system configured to employ one ablation method of the present invention.
- FIG. 10 is a representative view of a treatment site from along a longitudinal axis of a catheter.
- a visualization system/method that uses ICG dye for distinguishing ablated tissue from de novo tissue.
- ICG Indocyanine green
- ICG dye has the following formula:
- ICG dye is traditionally used for determining cardiac output, hepatic function, and liver blood flow, and for ophthalmic angiography. It has a peak spectral absorption at about 800 nm. These infrared frequencies penetrate retinal layers and other tissue allowing ICG angiography to image deeper patterns of circulation than fluorescein angiography. ICG binds tightly to plasma proteins and becomes confined to the vascular system. ICG has a half-life of 150 to 180 seconds and is removed from circulation exclusively by the liver to bile juice.
- ICG is a fluorescent dye which is used in medicine as an indicator substance (e.g. for photometric hepatic function diagnostics and fluorescence angiography) in cardiac, circulatory, hepatic and ophthalmic conditions. ICG is typically administered intravenously and, depending on liver performance, is eliminated from the body with a half-life of approximately 3-4 minutes. ICG sodium salt is normally available in powder form and can be dissolved in various solvents; 5% ( ⁇ 5% depending on batch) sodium iodide is usually added to ensure better solubility. The sterile lyophilisate of a water-ICG solution is approved in many European countries and the United States under the names ICG-Pulsion and IC-Green as a diagnostic for intravenous use.
- the absorption and fluorescence spectrum of ICG is in the near infrared region. Both depend to some degree on the solvent used and the concentration. ICG absorbs mainly between 600 nm and 900 nm and emits fluorescence between 750 nm and 950 nm. The large overlapping of the absorption and fluorescence spectra leads to a marked reabsorption of the fluorescence by ICG itself.
- the fluorescence spectrum is very wide. Its maximum values are approximately 810 nm in water and approximately 830 nm in blood. For medical applications based on absorption, the maximum absorption at approximately 800 nm (in blood plasma at low concentrations) is important.
- lasers with a wavelength of around 780 to 815 nm are used. At this wavelength, ICG still absorbs very well and yet it is still technically possible to suppress the excitation light in order to detect the fluorescence.
- FIG. 1 is a schematic block diagram illustrating an ablator/endoscopic system in accordance with the invention, designated generally by reference numeral 10 .
- Ablator system 10 preferably includes a surgical ablation instrument 100 preferably including an endoscope and ablation instrument as discussed below.
- the surgical ablation instrument 100 can be any number of different ablation instruments that are commercially available including those disclosed by Applicant in previous U.S. patents and patent applications (e.g., U.S. patent application publication Nos. 2009/0326320 and 2011/0082451, each of which is hereby incorporated by reference in its entirety).
- the ablation instrument 100 is of a type that emits ablation energy sufficient to cause formation of an ablation at a tissue target site.
- the ablator system 10 further preferably includes an aiming light source 20 and an illumination light source 24 .
- a processor 12 designed to accept input and output data from the connected instruments, display and controller and process that data into visual information.
- an excitation light source YY that emits light in the wavelength range adequate to excite the ICG dye fluorescence.
- the illumination light source 24 may be identical to the excitation source YY.
- the illumination light source 24 may provide a broadband white light illumination for normal endoscopic imaging and then be converted to an excitation light source by using an optical filter to remove wavelengths away from the absorption peak of ICG.
- an endoscope is preferably provided in ablation instrument 100 and has the capability of capturing both live images and recording still images.
- An illumination light is used to provide operating light to the surgical site.
- the illumination light is of a frequency that allows the user to differentiate between different tissues present at the operating site.
- An aiming light source 20 is used to visualize the location where energy will be delivered by the ablation instrument 100 to tissue. It is envisioned that the aiming light will be of a wavelength that can be recorded by an image capture device and visible on a display.
- the processor 12 is designed to process live visual data as well as data from the ablation instrument controllers and display.
- the processor is configured execute a series of software and/or hardware modules configured to interpret, manipulate and record visual information received from the surgical site.
- the processor 12 is further configured to manipulate and provide illustrative and graphical overlays and composite or hybrid visual data to the display device.
- the system 10 further includes a controller 16 , an energy source 18 , aiming light source 20 and a user interface 22 .
- Controller 16 is preferably configured to control the output of the energy source 18 and the illumination and excitation sources 24 and 25 of an energy transmitter as well as determine the distance and movement of an energy transmitter relative to tissue at an ablation surgical site (as discussed further below).
- an endoscope is preferably supported by the ablation instrument 100 and captures images that can be processed by the processor 12 to determine whether sufficient ablative energy deliveries have been directed to a specific area of a surgical site. Data obtained from the endoscope includes real-time video or still images of the surgical site as seen from the ablation instrument.
- the aiming light source 20 is used to visualize the surgical site location 120 where energy will be delivered by the ablation instrument 100 to tissue 130 .
- the aiming light source 20 outputs light in a visible region of the electromagnetic spectrum.
- the controller 16 transmits radiant energy, via energy source 18 , from the ablation instrument 100 to a target tissue site 120 to effect ablation by lesions.
- radiant energy as used herein is intended to encompass energy sources that do not rely primarily on conductive or convective heat transfer. Such sources include, but are not limited to, acoustic, laser and electromagnetic radiation sources and, more specifically, include microwave, x-ray, gamma-ray, ultrasonic and radiant light sources.
- the term “light” as used herein is intended to encompass electromagnetic radiation including, but not limited to, visible light, infrared and ultraviolet radiation.
- the illumination light source 24 is a light source used to provide proper illumination to the surgical site.
- the illuminate is configured so that natural biological tones and hues can be easily identifiable by an operator.
- the controller 16 can provide the user with the ability to control the function of the aiming light source, the user input devices, and the ablation instrument.
- the controller serves as the primary control interface for the ablation system. Through the controller, the user can turn on and off both the aiming and illumination lights. Furthermore the controller possesses the ability to change the illumination and aiming light intensity. The ability to switch user interfaces or display devices is also envisioned. Additionally, the controller gives access to the ablation instrument, including control over the intensity of the discharge, duration and location of ablative energy discharges.
- the controller 16 can further provide a safety shutoff to the system in the event that a clear transmission pathway between the radiant energy source and the target tissue is lost during energy delivery (e.g., see commonly owned U.S. patent application Ser. No. 12/896,010, filed Oct. 1, 2010, which is hereby incorporated by reference in its entirety.
- the controller can be separate microprocessor based control interface hardware or it can be a portion of a configured as a module operating through a processor based computer system configured to accept and control inputs from various physical devices.
- a set of modules cooperate with one another to provide the information presented through the interface of the system of FIG. 1 .
- an analysis module 218 there is an analysis module 218 , a multiple view module 220 , a composite module 222 , a mapping module 224 , an illustrating module 226 , and a control interface module 228 .
- Each of these modules can comprise hardware, code executing in a processor, or both, that configures a machines such as a workstation to implement the functionality described herein.
- the analysis module 218 includes instructions for analyzing a lesion and determining if it is sufficient for the desired treatment.
- the analysis module is configured to inspect the image data captured by the image capture device and a lesion of sufficient dimensions and quality has been formed.
- the analysis module 218 can be implemented as discrete sub-modules to provide functions such as receiving data on the duration and intensity of an ablative emission.
- An additional sub module is capable of evaluating the duration of the energy emission and comparing it to a look up table of sufficient duration and intensity values suitable to form a proper lesion.
- the multiple view module 220 includes instructions for configuring the processor 12 to provide multiple images to the display.
- the multiple view module configures the display to depict at least two image depiction areas. In a first image depiction area, the live video stream of the surgical site is displayed to the user. In a second image depiction area, a still image, highlighting the last target of ablative energy is depicted.
- the composite module 222 includes instructions for combining a series of still images and producing a composite image that depicts the target location of the ablative emission in each still image.
- the compositing module 222 can be implemented as discrete sub-modules to provide functions such as altering the transparency of each still image layer of the composite image so that a time based map of ablation locations can be produced. Another function implemented by the submodules is construction of a video or slideshow from a sequence of still images.
- the mapping module 224 includes instructions for overlaying proposed treatment paths on the live image.
- the mapping module is configured to show showing colored markers indicating acceptable levels of ablative energy depositing.
- the mapping module is capable of generating a green colored visual marker and superposing it over the live image to indicate areas that have yet to receive levels of ablative energy necessary for treatment.
- the mapping module 224 is also capable of simultaneously generating a red colored (or other color) visual marker and superimposing it over the live image to indicate areas that have received sufficient quantities of ablative energy suitable lesions.
- the mapping module 224 can be implemented as discrete sub-modules to provide functions such as receiving data on the duration and intensity of an ablative emission and correlating that specific instance to a specific stored image.
- the illustrating module 226 includes instructions for providing an image to the display, wherein the image is an illustration or graphical representation of the surgical site.
- the illustrating module 226 is configured to allow annotation of the illustrated image as well as comparison between the live image and the illustrated image. For example, and as shown in FIG. 8 , display 14 provides a first screen portion 610 depicting the actual surgical site 152 as viewed from endoscope 176 .
- Display 14 also illustrates a second screen portion 620 illustrating a graphical depiction of the surgical site 152 indicating the actual path of the energy transmitter 140 on the tissue at the surgical site wherein the path consists of a trace indicating the sufficiency of the formed lesions in which a solid trace 630 indicates sufficient lesions and a hashed trace 640 indicates insufficient lesions.
- the control module 220 includes instruction for orientating and accessing the functions of each of the other modules, as well as communicating with the controller and inputting information or manipulating the parameters of the data being displayed during operation.
- the manipulation and controlling functions can be implemented as discrete sub-modules with instructions for selecting operation modes, control interfaces, display orientation, recording modes, storage device location and data entry.
- the user refers to the live video feed from the image capture device to determine where to direct a radiant energy transmission.
- a live video image and a still image of the surgical site are depicted on the display.
- the processor 12 outputs to the display 14 at least two separately defined image depiction areas 204 , 206 .
- One image depiction area 204 is reserved for displaying live video transmitted from the surgical site 152 .
- At least one other image depiction area 206 is used to depict an image or a composite image comprised of several still images representing specific moments in time during the surgical procedure.
- the live video shown to the user will allow the user to see the reflection of the aiming light 218 and hence direct ablative energy.
- the first still image 210 depicted will be a still image captured at a point in time prior to the initiation of the first radiant energy emission. For instance, at a point in time prior to the emission of radiant energy, the image capture device records an image 210 of the surgical site 152 that depicts the surgical site 152 without the aiming light. By taking a still image 210 of the site, the user can record a baseline image of the surgical site before any treatment has been commenced. Furthermore, through the functions of the illustrative module, an illustration of the untouched 152 can be generated.
- a still image 210 is taken of the surgical site 152 .
- the characteristics of the ablative event e.g. information regarding the duration and intensity of the radiant of the energy emission
- the reflection the aiming light will be visible in the still image, providing a location indicator as to where the energy was directed.
- a series of these still images can be combined by using the composite module.
- the composite image is composed a series of individual images representing a specific period of time during the procedure, a time based map of the entire operation can also be produced in real time or for subsequent review.
- control interfaces 216 for accessing the control module.
- the control interfaces allow the user to select image style and opacity as well and initiating the functions of the other modules. Furthermore the functions of the controller 16 are also controllable from the control interface.
- the invention is not to be understood to be limited to the two image depiction areas discussed above with reference to FIG. 3 or 4 , but rather may encompass any number of image depiction areas in which the images and representations of the surgical site 152 can be reviewed.
- the images shown by the display 14 can be manipulated by the modules to illustrate the presence of sufficient or insufficient lesion formation.
- the display 14 may illustrate the image of the surgical site 152 viewed from the endoscope 176 wherein varying shades of grey and white depict tissue and lesions and in the event insufficient lesions are determined to be formed, or a red marker can be superimposed on the image of the surgical site 152 at the location where the insufficient lesion was determined.
- an audio signal may also be emitted from ablator system 10 causing further warning to the user.
- the modules of the system permit the surgeon to view all treatment segments forming the entire ablation arc to see if a continuous, uninterrupted ablation has been formed (or see if the ablation has the intended, desired shape). If there are visible gaps or other imperfections with the formed ablation, the surgeon can move the energy transmitter 140 to the proper location for retreatment of these areas until the desired ablation is formed. The process can then be repeated to determine and confirm that the gap was eliminated.
- mapping, analyzing and illustrating functions performed by the ablation system of the present invention overcome the disadvantages associated with prior ablation surgical procedures and results in increased ablation success rates due to a more optimal and more accurate viewing and quality determination of the spot lesions created to form the continuous ablation at the tissue location for the surgical site 152 .
- FIG. 5 provides a schematic, cross-sectional view of an ablation instrument 100 , including an elongate body 114 , a central lumen tubing 116 and a compliant balloon 126 inflatable via one or more ports 122 in the central tubing 116 .
- the central tubing 116 can also house an energy emitter that is capable of both axial movement and rotation within a lumen formed in the elongate body 114 .
- an energy emitter that is capable of both axial movement and rotation within a lumen formed in the elongate body 114 .
- the catheter body 114 also provides lumens 118 A and 118 B for extraction (or circulation) of an inflation fluid, an endoscope 176 and illumination and excitation fibers 128 A and 128 B.
- the ablation instrument 100 is preferably designed such that upon disposition within the heart (e.g., proximal to a pulmonary vein), the balloon 126 can be inflated such that a shoulder portion 150 of the balloon 126 will be urged into close proximity with a target region 152 of cardiac tissue.
- the energy emitter (or “lesion generator”) 140 can be positioned to delivery ablative energy to the target region 152 to form a continuous lesion.
- continuous in the context of a lesion is intended to mean a lesion that substantially blocks electrical conduction between tissue segments on opposite sides of the lesion.
- the radiant energy emitter 140 is shown in FIG. 2 disposed within the balloon 126 remotely from the target tissue (e.g., within a central lumen 116 of the catheter body 114 or otherwise disposed within the balloon).
- the radiant energy transmitter (ablation element) 140 includes at least one optical fiber coupled to a distal light projecting, optical element, which cooperate to project a spot of ablative light energy through the instrument 100 to the target site 152 (in FIG. 6 ).
- the catheter body 114 , projection balloon 126 and inflation/ablation fluids are all preferably substantially transparent to the radiant energy at the selected wavelength of the energy source as well as to the absorption and emission wavelengths of ICG dye to provide a low-loss transmission pathway from the radiant energy transmitter 140 to the target site 152 .
- balloon encompasses deformable hollow shapes which can be inflated into various configurations including spherical, obloid, tear drop, etc., shapes dependent upon the requirements of the body cavity.
- Such balloon elements can be elastic or simply capable of unfolding or unwrapping into an expanded state.
- the balloon can further encompass multiple chamber configurations.
- a reflectance sensor preferably an endoscope 176 capable of capturing an image of the target site 152 and/or the instrument position.
- the endoscope 176 is typically an optical fiber bundle with a lens or other optical coupler at its distal end to receive light.
- the reflectance sensor/endoscope can also include an illumination source, such one or more optical fibers coupled to a light source or sources. Alternatively illumination and excitation light may be delivered though separate optical fibers as indicated by 128 A in FIG. 2 . Endoscopes are available commercially from various sources.
- the endoscope can further include an optical head assembly, as detailed in more detail below, to increase the field of view.
- ablation element 140 and endoscope 176 are adapted for independent axial movement within the catheter body 14 .
- endoscope as used herein is intended to encompass optical imaging devices, generally, including but not limited to endoscopes, fiberscopes, cardioscopes, angioscopes and other optical fiber-based imaging devices. More generally, “endoscope” encompasses any light-guiding (or waveguide) structure capable of transmitting an “image” of an object to a location for viewing, such as display 14 .
- spot lesions are formed at the target site 152 by applying radiant energy from the energy transmitter 140 to target tissue.
- the applied radiant energy may be applied in an energy range from about 50 Joules/cm 2 to about 1000 Joules/cm 2 , or preferably from about 75 Joules/cm 2 to about 750 Joules/cm 2 .
- the power levels applied by the energy emitter can range from about 10 Watts/cm 2 to about 150 Watts/cm 2 and the duration of energy delivery can range from about 1 second to about 1 minute, preferably from about 5 seconds to about 45 seconds, or more preferably from about 10 to about 30 seconds. For example, for power levels between 10 and 75 Watts/cm 2 it can be advantageous to apply the radiant energy for about 30 seconds.
- the energy emitter 140 is a radiant energy emitter including at least one optical fiber coupled to a distal light projecting optical element, which cooperate to project a spot of ablative light energy through the instrument 100 to the target site 152 .
- the optical element can further comprise one or more lens elements and/or refractive elements capable of projecting a spot or arc-shaped beam of radiation.
- the lesion generator may generate an annulus or partial ring of ablative radiation, as described in more detail in commonly owned U.S. Pat. No. 6,423,055 issued Jul. 22, 2002, herein incorporated by reference for its disclosure related thereto.
- the ablation instrument 100 includes an aiming light preferably having a pulsed operating mode in which visible light from the aiming light unit is delivered in pulses to cause intermittent illumination of the tissue at the target site 152 . This gives the aiming light an appearance of being a blinking light.
- the surgeon is able to directly observe the tissue that is being treated at the target site 152 , using an endoscope, between the aiming light pulses.
- the endoscope 176 is used to determine the extent of tissue ablation by sensing the change in color of the tissue as it is ablated and at a time when the aiming beam is in an off cycle via the display 14 .
- the surgeon can observe the treated tissue to determine how the treatment is progressing since the endoscope 176 is used to determine the extent of tissue ablation by sensing the change in color of the tissue as it is ablated and at a time when the aiming beam is in an off cycle.
- the processor 12 of ablator system 10 obviates this problem by determining the quality of the lesion formed on the tissue at the target site 152 which may be viewed on monitor 14 and/or indicated to a surgeon visual overlay or audio cues.
- the method of operation for determining the quality of spot lesions at an ablation surgical site 152 will now be discussed.
- the processor 12 captures the image from endoscope 176 of the tissue being ablated at the surgical site.
- the processor 12 also captures information relating to the energy transmitter 140 from controller 16 .
- the captured energy transmitter 140 information includes: the amount of radiant energy (power) applied by energy transmitter 140 on the tissue at the surgical site 152 to form spot lesions; the distance the energy transmitter 140 is from tissue to be ablated via spot lesions; and the rate of movement of energy transmitter 140 relative to the tissue at the surgical site 152 . It is to be appreciated that aforesaid information captured regarding energy transmitter 140 is not to be understood to be limited thereto as more or less information may be captured that is necessary to determine the quality of the spot lesions formed on the tissue at the surgical site.
- the processor 12 then preferably uses algorithmic techniques to determine whether a sufficient spot lesion has just recently been formed on the tissue at the surgical site (step 320 ).
- algorithmic techniques to determine whether a sufficient spot lesion has just recently been formed on the tissue at the surgical site (step 320 ).
- the rate of movement of the energy transmitter 140 relative to the tissue at the surgical site 152 e.g., the amount of time that energy is applied to the tissue at a given location
- a determination is made as to whether a sufficient spot lesion has been formed on the tissue at a location which the energy transmitter is applying ablation energy thereto.
- a lookup table or other similar means may also be used by processor 12 for determining the aforesaid lesion quality.
- a spot lesion is to be understood as being sufficient when it comprises enough scar tissue effective to block the transmission of electrical signals therethrough.
- the processor 12 is preferably further operative and configured to provide a signal to the surgeon indicative of whether a sufficient spot lesion has been formed (step 330 ).
- This indicative signal may be provided in the event an insufficient or no spot lesion was formed on the tissue at the surgical site 152 that was subject to the energy transmitter 140 dispersing energy thereto.
- This indicative signal may be an audio and/or visual signal.
- the audio signal may consist of a warning tone and the visual signal may consist of a marker (e.g., color red) superimposed on the display 14 illustrating the surgical site 152 (provided via endoscope 176 ) at the location at which the insufficient spot lesion was determined.
- the aforesaid warning signal is promptly provided to the surgeon enabling the surgeon to revisit the tissue having the insufficient lesion and make proper adjustments with the energy transmitter 140 (e.g., apply more energy, close the distance between energy transmitter 140 and the surgical site and/or slow the movement of energy transmitter 140 relative to the surgical site) so as to now form sufficient lesions.
- FIG. 9 is a block diagram of one computer system 300 configured for employment of method 100 .
- System 300 includes a user interface 305 , a processor 310 , and a memory 315 .
- System 300 may be implemented on a general purpose microcomputer, such as one of the members of the Sun® Microsystems family of computer systems, one of the members of the IBM® Personal Computer family, one of the members of the Apple® Computer family, or a myriad other conventional workstations.
- system 300 is represented herein as a standalone system, it is not limited to such, but instead can be coupled to other computer systems via a network (not shown).
- Memory 315 is a memory for storing data and instructions suitable for controlling the operation of processor 310 .
- An implementation of memory 315 would include a random access memory (RAM), a hard drive and a read only memory (ROM).
- RAM random access memory
- ROM read only memory
- One of the components stored in memory 315 is a program 320 .
- Program 320 includes instructions for controlling processor 310 to execute method 100 .
- Program 320 may be implemented as a single module or as a plurality of modules that operate in cooperation with one another.
- Program 320 is contemplated as representing a software embodiment of the method described hereinabove.
- User interface 305 includes an input device, such as a keyboard, touch screen, tablet, or speech recognition subsystem, for enabling a user to communicate information and command selections to processor 310 .
- User interface 305 also includes an output device such as a display or a printer. In the case of a touch screen, the input and output functions are provided by the same structure.
- a cursor control such as a mouse, track-ball, or joy stick, allows the user to manipulate a cursor on the display for communicating additional information and command selections to processor 310 .
- Storage media 325 can be any conventional storage media such as a magnetic tape, an optical storage media, a compact disc, or a floppy disc. Alternatively, storage media 325 can be a random access memory, or other type of electronic storage, located on a remote storage system.
- an ICG dye composition is used for visualizing ablated tissue and allowing the ablated tissue to be visually distinguished from de-novo tissue.
- a suitable and biologically sufficient amount of ICG dye is delivered to the patient either immediately prior to performing the ablation procedure; during the ablative procedure or immediately after the ablation procedure.
- the timing and time period for delivering the ICG dye is sufficient to allow the ICG dye to travel through the bloodstream to the ablation tissue site where the ICG dye binds to plasma proteins and permit visualization of the ablated tissue since the ablated tissue (a lesion) is visually distinguishable from de novo tissue (non-ablated tissue) as a result of the binding properties of the ICG dye.
- the ICG dye after the ICG dye is injected into the patient's arm (e.g., through an IV) or is otherwise delivered into the patient, it travels through the bloodstream to the target tissue in less than 1 minute (e.g., in about 15 to 20 seconds).
- the ICG dye one of the properties of the ICG dye is that it binds to blood plasma protein and therefore, any tissue that absorbs the ICG dye (e.g., ICG binds with blood plasma protein) is readily distinguishable from tissue that does not absorb the ICG dye due to the difference in observable fluorescence.
- ablated tissue is tissue which has undergone coagulative necrosis due to energy being applied to the tissue. Unlike, the surrounding de-novo tissue, the ablated tissue does not have blood flowing therein and therefore, the ICG dye bound to blood plasma protein is carried into the ablated tissue to a far lesser extent than it is carried into de novo tissue. The result is that the ablated tissue does not absorb the ICG dye and is thus marked by a lack of fluorescence.
- FIG. 10 is a representative endoscopic view of a treatment site from along a longitudinal axis of the catheter.
- This view is preferably displayed on a display, such as a monitor and the ablated tissue is displayed in a visually distinguished manner relative to the de-novo (untreated) tissue.
- a display such as a monitor
- the ablated tissue is displayed in a visually distinguished manner relative to the de-novo (untreated) tissue.
- areas that contain blood such as blood in the pulmonary vein lumen and blood in the atrium, etc.
- the area of the ablated tissue has a darker appearance due to a lack of ICG dye.
- the ablated tissue is easily distinguishable from the surrounding blood rich areas since the areas of ablated tissue lack the fluorescence that is exhibited in the blood rich areas.
- the areas of blood/tissue are visually differentiated from the locations of the energy delivery (the formation of the lesions) by the use of cross-hatching.
- the catheter shaft and are also visually distinguished from the blood/tissue and the lesions (by cross-hatching).
- the cross-hatched areas that denote blood/tissue are the areas of fluorescence when the appropriate energy is applied to the surgical site to cause the area to fluoresce
- the ablation system 100 described herein is modified by the inclusion of an excitation light that emits light at the proper excitation wavelength (e.g., about 805 nm) instead of the use of a white light that is used in other ablation procedures.
- the device also includes an imaging device, such as a camera or the like, which includes appropriate filters and is constructed to be able to detect and record near IR light near the peak of the ICG emission spectra (i.e., about 835 nm) on out to the limit of the ICG dye fluorescence spectrum (i.e. 880 nm) while filtering out all of the excitation light to allow the emitted fluorescence to be visible as shown in FIG. 10 ).
- an imaging device such as a camera or the like, which includes appropriate filters and is constructed to be able to detect and record near IR light near the peak of the ICG emission spectra (i.e., about 835 nm) on out to the limit of the ICG dye fluorescence spectrum (i.e. 880
- the principle of fluorescence imaging using ICG dye involves the following steps.
- the tissue of interest is illuminated at a selected excitation wavelength (about 750 nm to about 805 nm) while observing it at longer emission wavelengths (e.g., over 815 nm in the case of 805 nm excitation).
- Filters are preferably used as part of the imaging device to prevent mixing of the excitation (strong) and fluorescing (weak) rays to sum at a sensor or the like that is part of the overall imaging system. Even if the fluorescene is only a small fraction of the excitation intensity, a surprisingly good signal to noise ratio (SNR) is attached.
- SNR signal to noise ratio
- the exact shape of the observed spectra can depend somewhat on the chemical environment and physical conditions of the ICG molecules like temperature and ICG concentration as well as the absorption spectra of the tissue through which some of the emitted light must pass.
- ICG interleukin-1 kinase
- ⁇ -lipoprotein lipids of lipoprotein complexes
- binding to protein proteins also shifts, slowly, taking several minutes, the absorption peak, at 780 nm, toward longer wavelengths, to 805 nm. It has been reported that absorption peak maximum was observed at 810 nm in the epidermal cell cultures, and at 805-810 nm in the human skin in vivo. The emission peak is also shifted similarly.
- the imaging system in accordance with the present invention includes an appropriate imaging device that is configured to monitor, in real time, the condition of the tissue at the surgical site and in particular, allow the physician to readily distinguish between ablated tissue and de novo tissue that has not been ablated.
- the imaging system allows the observed image to be displayed in real-time on a display and/or recorded and stored in memory.
- An endoscope can be used to obtain an image of the ablated tissue as described herein.
- the endoscope is inserted into the body and positioned adjacent the area of interest.
- An instrument is then used in combination with the endoscope to provide energy at an appropriate wavelength to cause the ICG dye within the subject tissue to fluoresce so that the image can be obtained.
- a second instrument can be used with the endoscope that permits the image of the fluorescing ICG dye within the tissue to be obtained.
- an optical device is connected to a CCD camera can be used in conjunction with the endoscopic procedures of the present invention. The optical device and the CCD camera permits the physician to view the target tissue in the heart.
- the device When the imaging device is in the form of a CCD camera, the device includes software and equipment that effectively filters light (reflected light) of certain wavelength(s) and in particular, the imaging device can include one or more video chips and corresponding bandpass filters and/or other filter arrangements that allow the fluorescence emission of the ICG dye to be filtered out and then further processed.
- a traditional filter e.g., a bandpass filter
- fluorescence imaging can be done so that both visible or excitation and fluorescence images are displayed together as one image.
- the fluorescence image along may contain only a few details so that the visible image greatly helps to locate the fluorescing parts with the help of landmarks seen in the visible image.
- the fluorescence channel is shown, rendered, in colors like vivid green, having a striking color contrast to the visible image of tissues.
- the type of visualization is especially important in intraoperational use, where the fluorescing parts, like blood veins and healthy de novo tissue, should be recognized easily and immediately.
- Image registration software can then be used to combine the two images in proper alignment.
- a gap formed along the length of the lesion is readily recognizable since the area of the gap will exhibit fluorescence, while the other sections of the lesion lack fluorescence and appear dark.
- a gap (break) A is present in the lesion and is readily and immediately discoverable by the surgeon when viewing the display due to the fact that the area A (the gap area) fluoresces, while the lesion has a dark color on the display.
- holes/gaps located along the lesion are easily seen due to these areas appearing as fluorescent “hot spots” relative to the adjacent dark areas which represent the formed lesion(s).
- the surgeon can then further ablate the tissue to close off the gap or otherwise correct the formed ablation such that a complete ablation is formed as desired.
- the surgeon can then check the video display after performing such additional ablation to make sure that the lesion is complete as represented by a continuous dark segment (lack of fluorescence) on the video display. In other words, once corrective action is taken and these fluorescent “hot spots” are eliminated by ablating the tissue at such location, the “hot spots” will disappear.
- the vivid fluorescent colors that indicate the lack of ablated tissue and instead show areas of blood flow and de-novo tissue allow the surgeon in real-time to see deficiencies in the formed lesion (ablation) and take immediate corrective action, thereby ensuring that the lesion (ablation) is fully formed and will act to block electrical signals as desired.
- U.S. patent application publication No. 2009/0326320 discloses other details of exemplary imaging systems and is hereby incorporated by reference in its entirety. It will be understood that one or more of the features disclosed in that document can be implemented in the imaging system of the present invention in that the imaging system can include more than one means for visualizing the surgical site and providing the user (surgeon) with helpful feedback and information concerning the quality of the lesion (i.e., whether the lesion is a continuous, uninterrupted structure, etc.).
Abstract
Description
- This application is based on and claims priority to U.S. Provisional Patent Application Ser. No. 61/985,142, filed on Apr. 28, 2014, the entire contents of which are respectively incorporated by reference as if set forth in its entirety herein.
- The present disclosure relates to ablation instruments and methods of use thereof, in particular to ablation catheters and methods for visualizing tissue using an ICG dye composition to identify and distinguish ablative tissue from de novo tissue.
- Cardiac arrhythmias (e.g., fibrillation) are irregularities in the normal beating pattern of the heart and can manifest themselves in either the atria or the ventricles of the heart. For example, atrial fibrillation is a form of arrhythmia characterized by rapid randomized contractions of atrial myocardium, causing an irregular, often rapid ventricular rate. The regular pumping function of the atria is replaced by a disorganized, ineffective quivering as a result of chaotic conduction of electrical signals through the upper chambers of the heart. Atrial fibrillation is often associated with other forms of cardiovascular disease, including congestive heart failure, rheumatic heart disease, coronary artery disease, left ventricular hypertrophy, cardiomyopathy, or hypertension.
- It is now understood that recurrent atrial fibrillation (paroxysmal and persistent) is triggered by rapidly firing tissue, (called “ectopic foci”), that are located in one or more of the four pulmonary veins, which attach to the rear of the left atrium. It has been found that atrial fibrillation may be cured by electrically isolating the pulmonary veins from the rest of the atrium.
- Various techniques have been employed for pulmonary vein isolation. A common purpose of each of these techniques is to replace cardiac muscle cells with scar tissue, which scar tissue cannot conduct normal electrical activity within the heart.
- In one known approach, circumferential ablation of tissue at the junction of the pulmonary veins and the left atrium has been practiced to treat atrial fibrillation. By ablating the heart tissue at selected locations, electrical conductivity from one segment to another can be blocked and the resulting segments become too small to sustain the fibrillatory process on their own.
- Several types of ablation devices have recently been proposed for creating lesions to treat cardiac arrhythmias. Many of the recently proposed ablation instruments are percutaneous devices that are designed to create such lesions from within the heart. Such devices are positioned in the heart by catheterization of the patient, e.g., by passing the ablation instrument into the heart via a blood vessel, such as the femoral vein.
- Typically, percutaneous devices are positioned with the assistance of a guide catheter and guide wire, which are first advanced into heart. In one common approach, a guide catheter or similar guide device is advanced through the vasculature and into the left atrium of the heart. A guide wire is then advanced toward a pulmonary vein. A catheter instrument with an expandable element is then advanced through the guide catheter and over the guide wire and into the pulmonary vein where the expandable element (e.g., a balloon) is inflated. The balloon includes a circumferential ablation element, e.g., an energy emitting device, such as a laser, disposed in the inner surface of the balloon, which performs the ablation procedure.
- It is noted that ablation near or within the pulmonary vein can result in complications. Overtreatment deep within a vein can result in stenosis (closure of the vein itself), necrosis or other structural damage, any of which can necessitate immediate open chest surgery. Conversely, undertreatment in which scar tissue formed is not continuous and/or insufficient to replace the cardiac muscles sought to be electrically isolated from the atrium will cause the surgical ablation procedure to be unsuccessful. Thus, repeating of the surgical ablation procedure is then required which is almost always undesirable.
- Currently, when laser energy has been applied to a region of tissue at an ostium of the PV there is little to no visible change to that region of tissue when viewed through an endoscope thereby presenting the problem of distinguishing treated tissue (e.g., lesion) from de novo tissue.
- The lesions are not visible for various reasons. For example, the ablation energy in these procedures typically penetrates deeply into the atrial tissue to create the lesion while leaving the endocardial surface relatively undamaged. Additionally, color video cameras are often not sensitive enough to discriminate the subtle color changes that distinguish treated and untreated tissue. Also, the light levels delivered to the site are limited since they typically travel to the treatment site via a small optical fiber thereby further hindering the ability of video cameras to visualize these distinctions.
- Thus, there remains a need in the art for systems and methods configured to accurately and immediately discriminate lesions from de novo tissue, thereby allowing the user (surgeon or more specifically and electrophysiologist or interventional radiologist) to take corrective action in real time to ensure a complete lesion is formed.
- The present invention is directed to the use of an indocyanine green (ICG dye) composition as part of an imaging system for distinguishing lesions from de novo tissue. A tissue ablation system for identification of a lesion formed by directed energy emission at a surgical site of a patient includes a source of an indocyanine green (ICG dye) composition for delivery into a body of the patient including to the surgical site. The system further includes a tissue ablation instrument for use at the surgical site. The instrument includes a movable directed first energy emitter configured to emit a variable amount of directed energy for ablating tissue and forming a lesion at the surgical site. A second energy emitter is provided for applying energy of a type and in an amount sufficient to cause the ICG composition to fluoresce. The system further includes an imaging device that is configured to obtain an image of the surgical site while the ICG fluoresces with the lesion being visually identifiable relative to de-novo tissue based on a lack of observable fluorescence at locations of the lesion, while the de-novo tissue is characterized by areas of fluorescence. A display, such as a computer monitor, displays the image in real time.
- Since the formed lesion is immediately and readily visually distinguishable from the de novo tissue and blood due to the bright fluorescence of the de novo tissue and blood versus the formed lesion being characterized by a lack of fluorescence, the user (surgeon) can detect deficiencies in the lesion, such as gaps or breaks in the lesion, and take immediate corrective measures.
- These and other aspects, features and benefits of the invention can be further appreciated from the accompanying drawings, which illustrate certain embodiments of the invention together with the detailed description thereof.
- The objects and features of the invention may be understood with reference to the following detailed description of an illustrative embodiment of the present invention taken together in conjunction with the accompanying drawings in which:
-
FIG. 1 is a block diagram depicting the components of an endoscope-guided cardiac ablation system according to the invention; -
FIG. 2 is a schematic view of the of the cardiac ablation instrument of the cardiac ablation system ofFIG. 1 ; -
FIG. 3 is a block diagram of the processor modules used in the cardiac ablation instrument. -
FIG. 4 illustrates a user interface in the form of a splint-screen arrangement for displaying information; -
FIG. 5 is a schematic view of the cardiac ablation instrument ofFIG. 2 shown in a treatment position at a surgical site in the pulmonary vein; -
FIG. 6 is a schematic view of the cardiac ablation instrument ofFIG. 2 with its compliant balloon inflated and its ablation element deployed at one of a plurality of locations; -
FIG. 7 is a flow diagram illustrating the steps performed by the ablator system ofFIG. 1 for determining the quality of lesions formed during a surgical ablation procedure; -
FIG. 8 is a screen shot of the display ofFIG. 1 depicting visual warning signals indicative of insufficient lesions; -
FIG. 9 is a block diagram of a computer system configured to employ one ablation method of the present invention; and -
FIG. 10 is a representative view of a treatment site from along a longitudinal axis of a catheter. - The present invention will now be described more fully with reference to the accompanying drawings, in which illustrated embodiments of the present invention are shown. The present invention is not limited in any way to any of the illustrated embodiments.
- In accordance with the present invention and as described in detail below, a visualization system/method that uses ICG dye for distinguishing ablated tissue from de novo tissue.
- Indocyanine green (ICG) is a cyanine dye used in medical diagnostics. ICG dye has the following formula:
- ICG dye is traditionally used for determining cardiac output, hepatic function, and liver blood flow, and for ophthalmic angiography. It has a peak spectral absorption at about 800 nm. These infrared frequencies penetrate retinal layers and other tissue allowing ICG angiography to image deeper patterns of circulation than fluorescein angiography. ICG binds tightly to plasma proteins and becomes confined to the vascular system. ICG has a half-life of 150 to 180 seconds and is removed from circulation exclusively by the liver to bile juice.
- ICG is a fluorescent dye which is used in medicine as an indicator substance (e.g. for photometric hepatic function diagnostics and fluorescence angiography) in cardiac, circulatory, hepatic and ophthalmic conditions. ICG is typically administered intravenously and, depending on liver performance, is eliminated from the body with a half-life of approximately 3-4 minutes. ICG sodium salt is normally available in powder form and can be dissolved in various solvents; 5% (<5% depending on batch) sodium iodide is usually added to ensure better solubility. The sterile lyophilisate of a water-ICG solution is approved in many European countries and the United States under the names ICG-Pulsion and IC-Green as a diagnostic for intravenous use.
- The absorption and fluorescence spectrum of ICG is in the near infrared region. Both depend to some degree on the solvent used and the concentration. ICG absorbs mainly between 600 nm and 900 nm and emits fluorescence between 750 nm and 950 nm. The large overlapping of the absorption and fluorescence spectra leads to a marked reabsorption of the fluorescence by ICG itself. The fluorescence spectrum is very wide. Its maximum values are approximately 810 nm in water and approximately 830 nm in blood. For medical applications based on absorption, the maximum absorption at approximately 800 nm (in blood plasma at low concentrations) is important. In combination with fluorescence detection, lasers with a wavelength of around 780 to 815 nm are used. At this wavelength, ICG still absorbs very well and yet it is still technically possible to suppress the excitation light in order to detect the fluorescence.
-
FIG. 1 is a schematic block diagram illustrating an ablator/endoscopic system in accordance with the invention, designated generally byreference numeral 10.Ablator system 10 preferably includes asurgical ablation instrument 100 preferably including an endoscope and ablation instrument as discussed below. Thesurgical ablation instrument 100 can be any number of different ablation instruments that are commercially available including those disclosed by Applicant in previous U.S. patents and patent applications (e.g., U.S. patent application publication Nos. 2009/0326320 and 2011/0082451, each of which is hereby incorporated by reference in its entirety). In general, theablation instrument 100 is of a type that emits ablation energy sufficient to cause formation of an ablation at a tissue target site. - The
ablator system 10 further preferably includes an aiminglight source 20 and anillumination light source 24. Aprocessor 12 designed to accept input and output data from the connected instruments, display and controller and process that data into visual information. Also included is an excitation light source YY that emits light in the wavelength range adequate to excite the ICG dye fluorescence. In some embodiments theillumination light source 24 may be identical to the excitation source YY. Alternatively theillumination light source 24 may provide a broadband white light illumination for normal endoscopic imaging and then be converted to an excitation light source by using an optical filter to remove wavelengths away from the absorption peak of ICG. - As will also be appreciated from the below discussion, an endoscope is preferably provided in
ablation instrument 100 and has the capability of capturing both live images and recording still images. An illumination light is used to provide operating light to the surgical site. The illumination light is of a frequency that allows the user to differentiate between different tissues present at the operating site. An aiminglight source 20 is used to visualize the location where energy will be delivered by theablation instrument 100 to tissue. It is envisioned that the aiming light will be of a wavelength that can be recorded by an image capture device and visible on a display. - Composite Imaging System
- The
processor 12 is designed to process live visual data as well as data from the ablation instrument controllers and display. The processor is configured execute a series of software and/or hardware modules configured to interpret, manipulate and record visual information received from the surgical site. Theprocessor 12 is further configured to manipulate and provide illustrative and graphical overlays and composite or hybrid visual data to the display device. - As seen in
FIG. 1 , thesystem 10 further includes acontroller 16, anenergy source 18, aiminglight source 20 and auser interface 22.Controller 16 is preferably configured to control the output of theenergy source 18 and the illumination andexcitation sources ablation instrument 100 and captures images that can be processed by theprocessor 12 to determine whether sufficient ablative energy deliveries have been directed to a specific area of a surgical site. Data obtained from the endoscope includes real-time video or still images of the surgical site as seen from the ablation instrument. - The aiming
light source 20 is used to visualize the surgical site location 120 where energy will be delivered by theablation instrument 100 to tissue 130. Preferably, the aiminglight source 20 outputs light in a visible region of the electromagnetic spectrum. If a suitable ablation path is seen by the user, thecontroller 16 transmits radiant energy, viaenergy source 18, from theablation instrument 100 to a target tissue site 120 to effect ablation by lesions. It is to be appreciated that the term “radiant energy” as used herein is intended to encompass energy sources that do not rely primarily on conductive or convective heat transfer. Such sources include, but are not limited to, acoustic, laser and electromagnetic radiation sources and, more specifically, include microwave, x-ray, gamma-ray, ultrasonic and radiant light sources. Additionally, the term “light” as used herein is intended to encompass electromagnetic radiation including, but not limited to, visible light, infrared and ultraviolet radiation. - The
illumination light source 24 is a light source used to provide proper illumination to the surgical site. The illuminate is configured so that natural biological tones and hues can be easily identifiable by an operator. - The
controller 16 can provide the user with the ability to control the function of the aiming light source, the user input devices, and the ablation instrument. The controller serves as the primary control interface for the ablation system. Through the controller, the user can turn on and off both the aiming and illumination lights. Furthermore the controller possesses the ability to change the illumination and aiming light intensity. The ability to switch user interfaces or display devices is also envisioned. Additionally, the controller gives access to the ablation instrument, including control over the intensity of the discharge, duration and location of ablative energy discharges. Thecontroller 16 can further provide a safety shutoff to the system in the event that a clear transmission pathway between the radiant energy source and the target tissue is lost during energy delivery (e.g., see commonly owned U.S. patent application Ser. No. 12/896,010, filed Oct. 1, 2010, which is hereby incorporated by reference in its entirety. - The controller can be separate microprocessor based control interface hardware or it can be a portion of a configured as a module operating through a processor based computer system configured to accept and control inputs from various physical devices.
- As shown in
FIG. 3 , a set of modules cooperate with one another to provide the information presented through the interface of the system ofFIG. 1 . Thus, for example, there is ananalysis module 218, amultiple view module 220, acomposite module 222, amapping module 224, an illustrating module 226, and acontrol interface module 228. Each of these modules can comprise hardware, code executing in a processor, or both, that configures a machines such as a workstation to implement the functionality described herein. - With further reference to
FIG. 3 , theanalysis module 218 includes instructions for analyzing a lesion and determining if it is sufficient for the desired treatment. The analysis module is configured to inspect the image data captured by the image capture device and a lesion of sufficient dimensions and quality has been formed. Theanalysis module 218 can be implemented as discrete sub-modules to provide functions such as receiving data on the duration and intensity of an ablative emission. An additional sub module is capable of evaluating the duration of the energy emission and comparing it to a look up table of sufficient duration and intensity values suitable to form a proper lesion. - The
multiple view module 220 includes instructions for configuring theprocessor 12 to provide multiple images to the display. The multiple view module configures the display to depict at least two image depiction areas. In a first image depiction area, the live video stream of the surgical site is displayed to the user. In a second image depiction area, a still image, highlighting the last target of ablative energy is depicted. - The
composite module 222 includes instructions for combining a series of still images and producing a composite image that depicts the target location of the ablative emission in each still image. Thecompositing module 222 can be implemented as discrete sub-modules to provide functions such as altering the transparency of each still image layer of the composite image so that a time based map of ablation locations can be produced. Another function implemented by the submodules is construction of a video or slideshow from a sequence of still images. - The
mapping module 224 includes instructions for overlaying proposed treatment paths on the live image. The mapping module is configured to show showing colored markers indicating acceptable levels of ablative energy depositing. For example the mapping module is capable of generating a green colored visual marker and superposing it over the live image to indicate areas that have yet to receive levels of ablative energy necessary for treatment. Conversely, themapping module 224 is also capable of simultaneously generating a red colored (or other color) visual marker and superimposing it over the live image to indicate areas that have received sufficient quantities of ablative energy suitable lesions. Themapping module 224 can be implemented as discrete sub-modules to provide functions such as receiving data on the duration and intensity of an ablative emission and correlating that specific instance to a specific stored image. - The illustrating module 226 includes instructions for providing an image to the display, wherein the image is an illustration or graphical representation of the surgical site. The illustrating module 226 is configured to allow annotation of the illustrated image as well as comparison between the live image and the illustrated image. For example, and as shown in
FIG. 8 ,display 14 provides a first screen portion 610 depicting the actualsurgical site 152 as viewed fromendoscope 176.Display 14 also illustrates asecond screen portion 620 illustrating a graphical depiction of thesurgical site 152 indicating the actual path of theenergy transmitter 140 on the tissue at the surgical site wherein the path consists of a trace indicating the sufficiency of the formed lesions in which asolid trace 630 indicates sufficient lesions and a hashedtrace 640 indicates insufficient lesions. - The
control module 220 includes instruction for orientating and accessing the functions of each of the other modules, as well as communicating with the controller and inputting information or manipulating the parameters of the data being displayed during operation. The manipulation and controlling functions can be implemented as discrete sub-modules with instructions for selecting operation modes, control interfaces, display orientation, recording modes, storage device location and data entry. - The user refers to the live video feed from the image capture device to determine where to direct a radiant energy transmission. Upon first use of the device, a live video image and a still image of the surgical site are depicted on the display. As seen in
FIG. 4 , theprocessor 12 outputs to thedisplay 14 at least two separately definedimage depiction areas image depiction area 204 is reserved for displaying live video transmitted from thesurgical site 152. At least one otherimage depiction area 206 is used to depict an image or a composite image comprised of several still images representing specific moments in time during the surgical procedure. - The live video shown to the user will allow the user to see the reflection of the aiming light 218 and hence direct ablative energy. It is envisioned that the first still image 210 depicted will be a still image captured at a point in time prior to the initiation of the first radiant energy emission. For instance, at a point in time prior to the emission of radiant energy, the image capture device records an image 210 of the
surgical site 152 that depicts thesurgical site 152 without the aiming light. By taking a still image 210 of the site, the user can record a baseline image of the surgical site before any treatment has been commenced. Furthermore, through the functions of the illustrative module, an illustration of the untouched 152 can be generated. During emission of radiant energy a still image 210 is taken of thesurgical site 152. The characteristics of the ablative event (e.g. information regarding the duration and intensity of the radiant of the energy emission) are stored and associated with the image depicting that specific emission. In addition, the reflection the aiming light will be visible in the still image, providing a location indicator as to where the energy was directed. A series of these still images can be combined by using the composite module. By modifying the opacity of each image, the reflected light of the aiming light for each ablative event will be visible in the composite image. In this way, acomplete record 220 of where energy was directed will becomes available. Furthermore, because the composite image is composed a series of individual images representing a specific period of time during the procedure, a time based map of the entire operation can also be produced in real time or for subsequent review. - Also visible in
FIG. 4 arecontrol interfaces 216 for accessing the control module. The control interfaces allow the user to select image style and opacity as well and initiating the functions of the other modules. Furthermore the functions of thecontroller 16 are also controllable from the control interface. - It is to be appreciated the invention is not to be understood to be limited to the two image depiction areas discussed above with reference to
FIG. 3 or 4, but rather may encompass any number of image depiction areas in which the images and representations of thesurgical site 152 can be reviewed. With reference toFIG. 8 the images shown by thedisplay 14 can be manipulated by the modules to illustrate the presence of sufficient or insufficient lesion formation. For instance, thedisplay 14 may illustrate the image of thesurgical site 152 viewed from theendoscope 176 wherein varying shades of grey and white depict tissue and lesions and in the event insufficient lesions are determined to be formed, or a red marker can be superimposed on the image of thesurgical site 152 at the location where the insufficient lesion was determined. Coincidently, an audio signal may also be emitted fromablator system 10 causing further warning to the user. - Therefore, if the user is not satisfied with the quality of the lesion produced, or the modules indicate that a sufficient lesion was not produced, the user can promptly redo the treatment of a specific tissue location (spot treatment). Conversely, if the modules indicate that a sufficient lesion was formed, the user can confidently move on to a new tissue location to continue the treatment thus saving time and effort by avoiding the need to more closely examine the tissue location that was just treated. Hence, once the entire treatment is performed, the modules of the system permit the surgeon to view all treatment segments forming the entire ablation arc to see if a continuous, uninterrupted ablation has been formed (or see if the ablation has the intended, desired shape). If there are visible gaps or other imperfections with the formed ablation, the surgeon can move the
energy transmitter 140 to the proper location for retreatment of these areas until the desired ablation is formed. The process can then be repeated to determine and confirm that the gap was eliminated. - As a result, the mapping, analyzing and illustrating functions performed by the ablation system of the present invention overcome the disadvantages associated with prior ablation surgical procedures and results in increased ablation success rates due to a more optimal and more accurate viewing and quality determination of the spot lesions created to form the continuous ablation at the tissue location for the
surgical site 152. - With reference now to
FIG. 5 , a description ofablation instrument 100 is provided.FIG. 5 provides a schematic, cross-sectional view of anablation instrument 100, including anelongate body 114, acentral lumen tubing 116 and acompliant balloon 126 inflatable via one ormore ports 122 in thecentral tubing 116. Thecentral tubing 116 can also house an energy emitter that is capable of both axial movement and rotation within a lumen formed in theelongate body 114. Additionally formed in the elongated body 114 (also referred to herein as the catheter body) there can be a plurality of additional lumens, through which certain devices or instruments can be passed. For example, thecatheter body 114 also provideslumens endoscope 176 and illumination andexcitation fibers - It should be understood that the embodiments illustrated in the drawings are only a few of the cardiac ablation instruments that can be utilized in accordance with the present invention. Further descriptions of other embodiments can be found, for example, in commonly owned, co-pending U.S. patent application Ser. No. 10/357,156, filed Feb. 3, 2003, U.S. patent application Ser. No. 09/924,393, filed Aug. 7, 2001, each of which is expressly incorporated by reference.
- With reference now to
FIGS. 5-6 , theablation instrument 100 is preferably designed such that upon disposition within the heart (e.g., proximal to a pulmonary vein), theballoon 126 can be inflated such that ashoulder portion 150 of theballoon 126 will be urged into close proximity with atarget region 152 of cardiac tissue. As shown inFIG. 4 , the energy emitter (or “lesion generator”) 140 can be positioned to delivery ablative energy to thetarget region 152 to form a continuous lesion. The term “continuous” in the context of a lesion is intended to mean a lesion that substantially blocks electrical conduction between tissue segments on opposite sides of the lesion. - The
radiant energy emitter 140 is shown inFIG. 2 disposed within theballoon 126 remotely from the target tissue (e.g., within acentral lumen 116 of thecatheter body 114 or otherwise disposed within the balloon). In one illustrated embodiment, the radiant energy transmitter (ablation element) 140 includes at least one optical fiber coupled to a distal light projecting, optical element, which cooperate to project a spot of ablative light energy through theinstrument 100 to the target site 152 (inFIG. 6 ). Thecatheter body 114,projection balloon 126 and inflation/ablation fluids are all preferably substantially transparent to the radiant energy at the selected wavelength of the energy source as well as to the absorption and emission wavelengths of ICG dye to provide a low-loss transmission pathway from theradiant energy transmitter 140 to thetarget site 152. It should be understood that the term “balloon” encompasses deformable hollow shapes which can be inflated into various configurations including spherical, obloid, tear drop, etc., shapes dependent upon the requirements of the body cavity. Such balloon elements can be elastic or simply capable of unfolding or unwrapping into an expanded state. The balloon can further encompass multiple chamber configurations. - Also disposed within the
instrument 100 is a reflectance sensor, preferably anendoscope 176 capable of capturing an image of thetarget site 152 and/or the instrument position. Theendoscope 176 is typically an optical fiber bundle with a lens or other optical coupler at its distal end to receive light. The reflectance sensor/endoscope can also include an illumination source, such one or more optical fibers coupled to a light source or sources. Alternatively illumination and excitation light may be delivered though separate optical fibers as indicated by 128A inFIG. 2 . Endoscopes are available commercially from various sources. The endoscope can further include an optical head assembly, as detailed in more detail below, to increase the field of view. In one illustrated embodiment,ablation element 140 andendoscope 176 are adapted for independent axial movement within thecatheter body 14. - The term “endoscope” as used herein is intended to encompass optical imaging devices, generally, including but not limited to endoscopes, fiberscopes, cardioscopes, angioscopes and other optical fiber-based imaging devices. More generally, “endoscope” encompasses any light-guiding (or waveguide) structure capable of transmitting an “image” of an object to a location for viewing, such as
display 14. - Preferably, spot lesions are formed at the
target site 152 by applying radiant energy from theenergy transmitter 140 to target tissue. The applied radiant energy may be applied in an energy range from about 50 Joules/cm2 to about 1000 Joules/cm2, or preferably from about 75 Joules/cm2 to about 750 Joules/cm2. The power levels applied by the energy emitter can range from about 10 Watts/cm2 to about 150 Watts/cm2 and the duration of energy delivery can range from about 1 second to about 1 minute, preferably from about 5 seconds to about 45 seconds, or more preferably from about 10 to about 30 seconds. For example, for power levels between 10 and 75 Watts/cm2 it can be advantageous to apply the radiant energy for about 30 seconds. Lesser durations, e.g., of 10 to 20 seconds, can be used for power levels of 75 to 150 Watts/cm2. It is to be understood the above figures are provided as examples and the energy, power and time duration figures set forth above are provided merely as examples and are not to be understood to be limited thereto. - In the illustrated embodiment of the
ablation instrument 100 shown inFIGS. 5-6 , theenergy emitter 140 is a radiant energy emitter including at least one optical fiber coupled to a distal light projecting optical element, which cooperate to project a spot of ablative light energy through theinstrument 100 to thetarget site 152. The optical element can further comprise one or more lens elements and/or refractive elements capable of projecting a spot or arc-shaped beam of radiation. Alternatively, the lesion generator may generate an annulus or partial ring of ablative radiation, as described in more detail in commonly owned U.S. Pat. No. 6,423,055 issued Jul. 22, 2002, herein incorporated by reference for its disclosure related thereto. - Since the radiant energy (e.g., a laser) emitted from the
energy emitter 140 is typically outside the visual light spectrum that can be detected by the human eye, theablation instrument 100 includes an aiming light preferably having a pulsed operating mode in which visible light from the aiming light unit is delivered in pulses to cause intermittent illumination of the tissue at thetarget site 152. This gives the aiming light an appearance of being a blinking light. By delivering the visible aiming light in pulses, the surgeon is able to directly observe the tissue that is being treated at thetarget site 152, using an endoscope, between the aiming light pulses. - During a surgical ablation procedure, the
endoscope 176 is used to determine the extent of tissue ablation by sensing the change in color of the tissue as it is ablated and at a time when the aiming beam is in an off cycle via thedisplay 14. In other words, between the blinking (pulses) of the aiming light, the surgeon can observe the treated tissue to determine how the treatment is progressing since theendoscope 176 is used to determine the extent of tissue ablation by sensing the change in color of the tissue as it is ablated and at a time when the aiming beam is in an off cycle. However, many conditions may cause the actual detection of change in color of tissue being ablated to be difficult and/or unreliable in regards to whether proper spot lesions are formed by theenergy transmitter 140 on the tissue at the ablationsurgical site 152. For instance, insufficient illumination at thesurgical site 152 can make it difficult, if not impossible, to ascertain whether proper spot lesions were formed at the surgical site as viewed ondisplay 14. - The
processor 12 ofablator system 10 obviates this problem by determining the quality of the lesion formed on the tissue at thetarget site 152 which may be viewed onmonitor 14 and/or indicated to a surgeon visual overlay or audio cues. With reference now to the flow diagram ofFIG. 7 , the method of operation for determining the quality of spot lesions at an ablationsurgical site 152 will now be discussed. - Starting at
step 300, theprocessor 12 captures the image fromendoscope 176 of the tissue being ablated at the surgical site. Atstep 310, theprocessor 12 also captures information relating to theenergy transmitter 140 fromcontroller 16. The capturedenergy transmitter 140 information includes: the amount of radiant energy (power) applied byenergy transmitter 140 on the tissue at thesurgical site 152 to form spot lesions; the distance theenergy transmitter 140 is from tissue to be ablated via spot lesions; and the rate of movement ofenergy transmitter 140 relative to the tissue at thesurgical site 152. It is to be appreciated that aforesaid information captured regardingenergy transmitter 140 is not to be understood to be limited thereto as more or less information may be captured that is necessary to determine the quality of the spot lesions formed on the tissue at the surgical site. Theprocessor 12 then preferably uses algorithmic techniques to determine whether a sufficient spot lesion has just recently been formed on the tissue at the surgical site (step 320). In other words, given the distance theenergy transmitter 140 is located from the tissue at thesurgical site 152, the rate of movement of theenergy transmitter 140 relative to the tissue at the surgical site 152 (e.g., the amount of time that energy is applied to the tissue at a given location), and the amount of energy being applied, a determination is made as to whether a sufficient spot lesion has been formed on the tissue at a location which the energy transmitter is applying ablation energy thereto. A lookup table or other similar means may also be used byprocessor 12 for determining the aforesaid lesion quality. A spot lesion is to be understood as being sufficient when it comprises enough scar tissue effective to block the transmission of electrical signals therethrough. - The
processor 12 is preferably further operative and configured to provide a signal to the surgeon indicative of whether a sufficient spot lesion has been formed (step 330). This indicative signal may be provided in the event an insufficient or no spot lesion was formed on the tissue at thesurgical site 152 that was subject to theenergy transmitter 140 dispersing energy thereto. This indicative signal may be an audio and/or visual signal. The audio signal may consist of a warning tone and the visual signal may consist of a marker (e.g., color red) superimposed on thedisplay 14 illustrating the surgical site 152 (provided via endoscope 176) at the location at which the insufficient spot lesion was determined. Thus, whenimage processor 12 determines an insufficient spot lesion has been formed, the aforesaid warning signal is promptly provided to the surgeon enabling the surgeon to revisit the tissue having the insufficient lesion and make proper adjustments with the energy transmitter 140 (e.g., apply more energy, close the distance betweenenergy transmitter 140 and the surgical site and/or slow the movement ofenergy transmitter 140 relative to the surgical site) so as to now form sufficient lesions. -
FIG. 9 is a block diagram of onecomputer system 300 configured for employment ofmethod 100.System 300 includes a user interface 305, aprocessor 310, and amemory 315.System 300 may be implemented on a general purpose microcomputer, such as one of the members of the Sun® Microsystems family of computer systems, one of the members of the IBM® Personal Computer family, one of the members of the Apple® Computer family, or a myriad other conventional workstations. Althoughsystem 300 is represented herein as a standalone system, it is not limited to such, but instead can be coupled to other computer systems via a network (not shown). -
Memory 315 is a memory for storing data and instructions suitable for controlling the operation ofprocessor 310. An implementation ofmemory 315 would include a random access memory (RAM), a hard drive and a read only memory (ROM). One of the components stored inmemory 315 is aprogram 320. -
Program 320 includes instructions for controllingprocessor 310 to executemethod 100.Program 320 may be implemented as a single module or as a plurality of modules that operate in cooperation with one another.Program 320 is contemplated as representing a software embodiment of the method described hereinabove. - User interface 305 includes an input device, such as a keyboard, touch screen, tablet, or speech recognition subsystem, for enabling a user to communicate information and command selections to
processor 310. User interface 305 also includes an output device such as a display or a printer. In the case of a touch screen, the input and output functions are provided by the same structure. A cursor control such as a mouse, track-ball, or joy stick, allows the user to manipulate a cursor on the display for communicating additional information and command selections toprocessor 310. - While
program 320 is indicated as already loaded intomemory 315, it may be configured on astorage media 325 for subsequent loading intomemory 315.Storage media 325 can be any conventional storage media such as a magnetic tape, an optical storage media, a compact disc, or a floppy disc. Alternatively,storage media 325 can be a random access memory, or other type of electronic storage, located on a remote storage system. - The methods described herein have been indicated in connection with flow diagrams that facilitate a description of the principal processes; however, certain blocks can be invoked in an arbitrary order, such as when the events drive the program flow such as in an object-oriented program. Accordingly, the flow diagram is to be understood as an example flow and that the blocks can be invoked in a different order than as illustrated.
- It should be understood that various combination, alternatives and modifications of the present invention could be devised by those skilled in the art. The present invention is intended to embrace all such alternatives, modifications and variances that fall within the scope of the appended claims.
- Although described in connection with cardiac ablation procedures, it should be clear that the instruments and systems of the present invention can be used for a variety of other procedures where treatment with radiant energy is desirable, including laparoscopic, endoluminal, perivisceral, endoscopic, thoracoscopic, intra-articular and hybrid approaches.
- Use of ICG Dye for Visualization of Treated Tissue
- In accordance with the present invention, an ICG dye composition is used for visualizing ablated tissue and allowing the ablated tissue to be visually distinguished from de-novo tissue.
- A suitable and biologically sufficient amount of ICG dye is delivered to the patient either immediately prior to performing the ablation procedure; during the ablative procedure or immediately after the ablation procedure. The timing and time period for delivering the ICG dye is sufficient to allow the ICG dye to travel through the bloodstream to the ablation tissue site where the ICG dye binds to plasma proteins and permit visualization of the ablated tissue since the ablated tissue (a lesion) is visually distinguishable from de novo tissue (non-ablated tissue) as a result of the binding properties of the ICG dye.
- Accordingly, after the ICG dye is injected into the patient's arm (e.g., through an IV) or is otherwise delivered into the patient, it travels through the bloodstream to the target tissue in less than 1 minute (e.g., in about 15 to 20 seconds). As discussed herein, one of the properties of the ICG dye is that it binds to blood plasma protein and therefore, any tissue that absorbs the ICG dye (e.g., ICG binds with blood plasma protein) is readily distinguishable from tissue that does not absorb the ICG dye due to the difference in observable fluorescence.
- As is understood, ablated tissue is tissue which has undergone coagulative necrosis due to energy being applied to the tissue. Unlike, the surrounding de-novo tissue, the ablated tissue does not have blood flowing therein and therefore, the ICG dye bound to blood plasma protein is carried into the ablated tissue to a far lesser extent than it is carried into de novo tissue. The result is that the ablated tissue does not absorb the ICG dye and is thus marked by a lack of fluorescence.
-
FIG. 10 is a representative endoscopic view of a treatment site from along a longitudinal axis of the catheter. This view is preferably displayed on a display, such as a monitor and the ablated tissue is displayed in a visually distinguished manner relative to the de-novo (untreated) tissue. In particular and as a result of the use of the ICG dye, areas that contain blood (such as blood in the pulmonary vein lumen and blood in the atrium, etc.) are represented by high levels of fluorescence (which is graphically represented in the figure), while the area of the ablated tissue has a darker appearance due to a lack of ICG dye. In other words, the ablated tissue is easily distinguishable from the surrounding blood rich areas since the areas of ablated tissue lack the fluorescence that is exhibited in the blood rich areas. - In
FIG. 10 , the areas of blood/tissue are visually differentiated from the locations of the energy delivery (the formation of the lesions) by the use of cross-hatching. The catheter shaft and are also visually distinguished from the blood/tissue and the lesions (by cross-hatching). As discussed herein, inFIG. 10 , the cross-hatched areas that denote blood/tissue are the areas of fluorescence when the appropriate energy is applied to the surgical site to cause the area to fluoresce - The
ablation system 100 described herein is modified by the inclusion of an excitation light that emits light at the proper excitation wavelength (e.g., about 805 nm) instead of the use of a white light that is used in other ablation procedures. The device also includes an imaging device, such as a camera or the like, which includes appropriate filters and is constructed to be able to detect and record near IR light near the peak of the ICG emission spectra (i.e., about 835 nm) on out to the limit of the ICG dye fluorescence spectrum (i.e. 880 nm) while filtering out all of the excitation light to allow the emitted fluorescence to be visible as shown inFIG. 10 ). - The principle of fluorescence imaging using ICG dye involves the following steps. The tissue of interest is illuminated at a selected excitation wavelength (about 750 nm to about 805 nm) while observing it at longer emission wavelengths (e.g., over 815 nm in the case of 805 nm excitation). Filters are preferably used as part of the imaging device to prevent mixing of the excitation (strong) and fluorescing (weak) rays to sum at a sensor or the like that is part of the overall imaging system. Even if the fluorescene is only a small fraction of the excitation intensity, a surprisingly good signal to noise ratio (SNR) is attached. A brightly fluorescing object (mostly blood and well perfused tissue) can be seen on a display. Without the use of filters, a weak fluorescene image cannot be seen among the strong reflection of the excitation light.
- ICG fluoresces at about 800 nm and longer wavelengths. The exact shape of the observed spectra can depend somewhat on the chemical environment and physical conditions of the ICG molecules like temperature and ICG concentration as well as the absorption spectra of the tissue through which some of the emitted light must pass.
- One of the advantageous properties of ICG is the fast binding to plasma proteins, especially lipoproteins, makes repeated intraoperational applications of ICG possible. The binding to plasma proteins does not alter the protein structures, which is one sign of nontoxicity. It is believed that ICG binds to the lipids of lipoprotein complexes (β-lipoprotein), and that the bind results in more intense fluorescence than ICG bound to for example, free cholesterol. Binding to protein proteins also shifts, slowly, taking several minutes, the absorption peak, at 780 nm, toward longer wavelengths, to 805 nm. It has been reported that absorption peak maximum was observed at 810 nm in the epidermal cell cultures, and at 805-810 nm in the human skin in vivo. The emission peak is also shifted similarly.
- The Imaging System
- The imaging system in accordance with the present invention includes an appropriate imaging device that is configured to monitor, in real time, the condition of the tissue at the surgical site and in particular, allow the physician to readily distinguish between ablated tissue and de novo tissue that has not been ablated. The imaging system allows the observed image to be displayed in real-time on a display and/or recorded and stored in memory.
- An endoscope can be used to obtain an image of the ablated tissue as described herein. The endoscope is inserted into the body and positioned adjacent the area of interest. An instrument is then used in combination with the endoscope to provide energy at an appropriate wavelength to cause the ICG dye within the subject tissue to fluoresce so that the image can be obtained. Similarly, a second instrument can be used with the endoscope that permits the image of the fluorescing ICG dye within the tissue to be obtained. For example, an optical device is connected to a CCD camera can be used in conjunction with the endoscopic procedures of the present invention. The optical device and the CCD camera permits the physician to view the target tissue in the heart. When the imaging device is in the form of a CCD camera, the device includes software and equipment that effectively filters light (reflected light) of certain wavelength(s) and in particular, the imaging device can include one or more video chips and corresponding bandpass filters and/or other filter arrangements that allow the fluorescence emission of the ICG dye to be filtered out and then further processed. As is known, a traditional filter (e.g., a bandpass filter) can be tailored to a specific waveband of a certain width and is centered at a specific wavelength (i.e., the fluorescence emission).
- Combined Visible and Fluorescence Images
- According to one embodiment, fluorescence imaging can be done so that both visible or excitation and fluorescence images are displayed together as one image. The fluorescence image along may contain only a few details so that the visible image greatly helps to locate the fluorescing parts with the help of landmarks seen in the visible image. Typically, the fluorescence channel is shown, rendered, in colors like vivid green, having a striking color contrast to the visible image of tissues. The type of visualization is especially important in intraoperational use, where the fluorescing parts, like blood veins and healthy de novo tissue, should be recognized easily and immediately. Image registration software can then be used to combine the two images in proper alignment.
- Review of Ablation Quality
- The present invention thus allows the surgeon to view the formed ablation(s) (lesion) in real-time and to evaluate the quality of the formed ablation(s) to allow the surgeon to decide whether additional ablation treatment is needed. For example, if the surgeon views the display and notices that the formed ablation(s) includes a defect, such as a void (gap or break) along its length, or is otherwise not acceptable, then the
- A gap formed along the length of the lesion is readily recognizable since the area of the gap will exhibit fluorescence, while the other sections of the lesion lack fluorescence and appear dark. In
FIG. 10 , a gap (break) A is present in the lesion and is readily and immediately discoverable by the surgeon when viewing the display due to the fact that the area A (the gap area) fluoresces, while the lesion has a dark color on the display. Thus, holes/gaps located along the lesion are easily seen due to these areas appearing as fluorescent “hot spots” relative to the adjacent dark areas which represent the formed lesion(s). - After viewing the display, the surgeon can then further ablate the tissue to close off the gap or otherwise correct the formed ablation such that a complete ablation is formed as desired. The surgeon can then check the video display after performing such additional ablation to make sure that the lesion is complete as represented by a continuous dark segment (lack of fluorescence) on the video display. In other words, once corrective action is taken and these fluorescent “hot spots” are eliminated by ablating the tissue at such location, the “hot spots” will disappear. The vivid fluorescent colors that indicate the lack of ablated tissue and instead show areas of blood flow and de-novo tissue allow the surgeon in real-time to see deficiencies in the formed lesion (ablation) and take immediate corrective action, thereby ensuring that the lesion (ablation) is fully formed and will act to block electrical signals as desired.
- U.S. patent application publication No. 2009/0326320 discloses other details of exemplary imaging systems and is hereby incorporated by reference in its entirety. It will be understood that one or more of the features disclosed in that document can be implemented in the imaging system of the present invention in that the imaging system can include more than one means for visualizing the surgical site and providing the user (surgeon) with helpful feedback and information concerning the quality of the lesion (i.e., whether the lesion is a continuous, uninterrupted structure, etc.).
- One skilled in the art will appreciate further features and advantages of the invention based on the above-described embodiments. Accordingly, the invention is not to be limited by what has been particularly shown and described, except as indicated by the appended claims. All publications and references cited herein are expressly incorporated herein by reference in their entirety.
Claims (18)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/697,065 US20150305604A1 (en) | 2014-04-28 | 2015-04-27 | System and method for visualizing tissue with an icg dye composition during ablation procedures |
US16/259,483 US11246476B2 (en) | 2014-04-28 | 2019-01-28 | Method for visualizing tissue with an ICG dye composition during ablation procedures |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201461985142P | 2014-04-28 | 2014-04-28 | |
US14/697,065 US20150305604A1 (en) | 2014-04-28 | 2015-04-27 | System and method for visualizing tissue with an icg dye composition during ablation procedures |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/259,483 Division US11246476B2 (en) | 2014-04-28 | 2019-01-28 | Method for visualizing tissue with an ICG dye composition during ablation procedures |
Publications (1)
Publication Number | Publication Date |
---|---|
US20150305604A1 true US20150305604A1 (en) | 2015-10-29 |
Family
ID=54333618
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/697,065 Abandoned US20150305604A1 (en) | 2014-04-28 | 2015-04-27 | System and method for visualizing tissue with an icg dye composition during ablation procedures |
US16/259,483 Active 2036-01-12 US11246476B2 (en) | 2014-04-28 | 2019-01-28 | Method for visualizing tissue with an ICG dye composition during ablation procedures |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/259,483 Active 2036-01-12 US11246476B2 (en) | 2014-04-28 | 2019-01-28 | Method for visualizing tissue with an ICG dye composition during ablation procedures |
Country Status (4)
Country | Link |
---|---|
US (2) | US20150305604A1 (en) |
EP (1) | EP3137007A4 (en) |
JP (1) | JP2017513645A (en) |
WO (1) | WO2015167929A1 (en) |
Cited By (55)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20170235118A1 (en) * | 2016-02-15 | 2017-08-17 | Leica Instruments (Singapore) Pte. Ltd. | Illumination filter system and observation system for a multispectral fluorescence microscope, multispectral fluorescence microscope, and microscopying method |
JP2019042156A (en) * | 2017-09-01 | 2019-03-22 | 富士フイルム株式会社 | Medical image processing apparatus, endoscope apparatus, diagnosis support apparatus, and medical service support apparatus |
US20190122345A1 (en) * | 2016-04-04 | 2019-04-25 | Sony Corporation | Image processing apparatus, imaging apparatus, image processing method, and program |
USD851245S1 (en) | 2017-04-14 | 2019-06-11 | Cardiofocus, Inc. | Compliant balloon |
CN110510147A (en) * | 2019-08-02 | 2019-11-29 | 西安飞机工业(集团)有限责任公司 | A kind of aircaft configuration crack detecting method |
US20200037925A1 (en) * | 2013-09-06 | 2020-02-06 | Covidien Lp | System and method for light based lung visualization |
CN111526776A (en) * | 2017-12-27 | 2020-08-11 | 爱惜康有限责任公司 | Fluorescence imaging in low light environments |
WO2022031615A1 (en) * | 2020-08-06 | 2022-02-10 | Medtronic Navigation, Inc. | Tumor ablation planning using interstitial optical mapping |
US11246476B2 (en) * | 2014-04-28 | 2022-02-15 | Cardiofocus, Inc. | Method for visualizing tissue with an ICG dye composition during ablation procedures |
US11266304B2 (en) | 2019-06-20 | 2022-03-08 | Cilag Gmbh International | Minimizing image sensor input/output in a pulsed hyperspectral imaging system |
US11276148B2 (en) | 2019-06-20 | 2022-03-15 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed fluorescence imaging system |
US20220079600A1 (en) * | 2020-09-15 | 2022-03-17 | Baylis Medical Company Inc. | Medical guidewire assembly |
US11280737B2 (en) | 2019-06-20 | 2022-03-22 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed fluorescence imaging system |
US11284784B2 (en) | 2019-06-20 | 2022-03-29 | Cilag Gmbh International | Controlling integral energy of a laser pulse in a fluorescence imaging system |
US11288772B2 (en) | 2019-06-20 | 2022-03-29 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed fluorescence imaging system |
US20220142708A1 (en) * | 2020-11-12 | 2022-05-12 | Cardiofocus, Inc. | Ablation Catheters with Multiple Endoscopes and Imaging Chip Endoscopes and System for Altering an Orientation of an Endoscopic Image |
US11344365B2 (en) | 2016-01-05 | 2022-05-31 | Cardiofocus, Inc. | Ablation system with automated sweeping ablation energy element |
US11389236B2 (en) | 2018-01-15 | 2022-07-19 | Cardiofocus, Inc. | Ablation system with automated ablation energy element |
US11389066B2 (en) | 2019-06-20 | 2022-07-19 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed hyperspectral, fluorescence, and laser mapping imaging system |
US11398011B2 (en) | 2019-06-20 | 2022-07-26 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed laser mapping imaging system |
US11399717B2 (en) | 2019-06-20 | 2022-08-02 | Cilag Gmbh International | Hyperspectral and fluorescence imaging and topology laser mapping with minimal area monolithic image sensor |
US11412152B2 (en) | 2019-06-20 | 2022-08-09 | Cilag Gmbh International | Speckle removal in a pulsed hyperspectral imaging system |
US11412920B2 (en) * | 2019-06-20 | 2022-08-16 | Cilag Gmbh International | Speckle removal in a pulsed fluorescence imaging system |
US11432706B2 (en) | 2019-06-20 | 2022-09-06 | Cilag Gmbh International | Hyperspectral imaging with minimal area monolithic image sensor |
US11477390B2 (en) | 2019-06-20 | 2022-10-18 | Cilag Gmbh International | Fluorescence imaging with minimal area monolithic image sensor |
US11471055B2 (en) | 2019-06-20 | 2022-10-18 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed fluorescence imaging system |
WO2022212849A3 (en) * | 2021-04-01 | 2022-11-10 | Cardiofocus, Inc. | Deployable structures to provide electrodes on the surface of an endoscopically guided laser ablation catheter |
US11516388B2 (en) | 2019-06-20 | 2022-11-29 | Cilag Gmbh International | Pulsed illumination in a fluorescence imaging system |
US11516387B2 (en) | 2019-06-20 | 2022-11-29 | Cilag Gmbh International | Image synchronization without input clock and data transmission clock in a pulsed hyperspectral, fluorescence, and laser mapping imaging system |
US11531112B2 (en) | 2019-06-20 | 2022-12-20 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a hyperspectral, fluorescence, and laser mapping imaging system |
US11533417B2 (en) | 2019-06-20 | 2022-12-20 | Cilag Gmbh International | Laser scanning and tool tracking imaging in a light deficient environment |
US11540696B2 (en) | 2019-06-20 | 2023-01-03 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed fluorescence imaging system |
US11550057B2 (en) | 2019-06-20 | 2023-01-10 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a fluorescence imaging system |
US11612309B2 (en) | 2019-06-20 | 2023-03-28 | Cilag Gmbh International | Hyperspectral videostroboscopy of vocal cords |
US11617541B2 (en) | 2019-06-20 | 2023-04-04 | Cilag Gmbh International | Optical fiber waveguide in an endoscopic system for fluorescence imaging |
US11622094B2 (en) | 2019-06-20 | 2023-04-04 | Cilag Gmbh International | Wide dynamic range using a monochrome image sensor for fluorescence imaging |
US11624830B2 (en) | 2019-06-20 | 2023-04-11 | Cilag Gmbh International | Wide dynamic range using a monochrome image sensor for laser mapping imaging |
US11633089B2 (en) | 2019-06-20 | 2023-04-25 | Cilag Gmbh International | Fluorescence imaging with minimal area monolithic image sensor |
US11668920B2 (en) | 2019-06-20 | 2023-06-06 | Cilag Gmbh International | Driving light emissions according to a jitter specification in a fluorescence imaging system |
US11671691B2 (en) | 2019-06-20 | 2023-06-06 | Cilag Gmbh International | Image rotation in an endoscopic laser mapping imaging system |
US11674848B2 (en) | 2019-06-20 | 2023-06-13 | Cilag Gmbh International | Wide dynamic range using a monochrome image sensor for hyperspectral imaging |
US11700995B2 (en) | 2019-06-20 | 2023-07-18 | Cilag Gmbh International | Speckle removal in a pulsed fluorescence imaging system |
US11716533B2 (en) | 2019-06-20 | 2023-08-01 | Cilag Gmbh International | Image synchronization without input clock and data transmission clock in a pulsed fluorescence imaging system |
US11716543B2 (en) | 2019-06-20 | 2023-08-01 | Cilag Gmbh International | Wide dynamic range using a monochrome image sensor for fluorescence imaging |
US11758256B2 (en) | 2019-06-20 | 2023-09-12 | Cilag Gmbh International | Fluorescence imaging in a light deficient environment |
US11793399B2 (en) | 2019-06-20 | 2023-10-24 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed hyperspectral imaging system |
US11821989B2 (en) | 2019-06-20 | 2023-11-21 | Cllag GmbH International | Hyperspectral, fluorescence, and laser mapping imaging with fixed pattern noise cancellation |
US11854175B2 (en) | 2019-06-20 | 2023-12-26 | Cilag Gmbh International | Fluorescence imaging with fixed pattern noise cancellation |
US11877065B2 (en) | 2019-06-20 | 2024-01-16 | Cilag Gmbh International | Image rotation in an endoscopic hyperspectral imaging system |
US11892403B2 (en) | 2019-06-20 | 2024-02-06 | Cilag Gmbh International | Image synchronization without input clock and data transmission clock in a pulsed fluorescence imaging system |
US11898909B2 (en) | 2019-06-20 | 2024-02-13 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed fluorescence imaging system |
US11903563B2 (en) | 2019-06-20 | 2024-02-20 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a fluorescence imaging system |
US11925328B2 (en) | 2019-06-20 | 2024-03-12 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed hyperspectral imaging system |
US11931009B2 (en) | 2019-06-20 | 2024-03-19 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a hyperspectral imaging system |
US11937784B2 (en) | 2019-06-20 | 2024-03-26 | Cilag Gmbh International | Fluorescence imaging in a light deficient environment |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11957314B2 (en) * | 2017-02-18 | 2024-04-16 | University Of Rochester | Surgical visualization and medical imaging devices and methods using near infrared fluorescent polymers |
JP2020168208A (en) * | 2019-04-03 | 2020-10-15 | オリンパス株式会社 | Endoscope system |
WO2021039869A1 (en) * | 2019-08-28 | 2021-03-04 | ソニー・オリンパスメディカルソリューションズ株式会社 | Medical image processing device and medical observation system |
KR102095794B1 (en) * | 2019-10-28 | 2020-04-02 | 오리오스메디칼 주식회사 | Method and apparatus for scanning blood vessels |
CN116249504A (en) * | 2020-09-29 | 2023-06-09 | 奥林巴斯株式会社 | Auxiliary device, endoscope system, auxiliary method, and program |
WO2022070275A1 (en) * | 2020-09-29 | 2022-04-07 | オリンパス株式会社 | Support device, endoscopic system, support method, and program |
Citations (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4336809A (en) * | 1980-03-17 | 1982-06-29 | Burleigh Instruments, Inc. | Human and animal tissue photoradiation system and method |
US5773835A (en) * | 1996-06-07 | 1998-06-30 | Rare Earth Medical, Inc. | Fiber optic spectroscopy |
US5775327A (en) * | 1995-06-07 | 1998-07-07 | Cardima, Inc. | Guiding catheter for the coronary sinus |
US5845646A (en) * | 1996-11-05 | 1998-12-08 | Lemelson; Jerome | System and method for treating select tissue in a living being |
US20020029062A1 (en) * | 2000-09-07 | 2002-03-07 | Shutaro Satake | Balloon catheter for pulmonary vein isolation |
US20020173785A1 (en) * | 2000-03-31 | 2002-11-21 | Medtronic, Inc. | System and method for positioning implantable medical devices within coronary veins |
US20030069620A1 (en) * | 2001-10-09 | 2003-04-10 | Hong Li | Balloon catheters for non-continuous lesions |
US20040186351A1 (en) * | 1996-11-20 | 2004-09-23 | Olympus Optical Co., Ltd. (Now Olympus Corporation) | Fluorescent endoscope system enabling simultaneous achievement of normal light observation based on reflected light and fluorescence observation based on light with wavelengths in infrared spectrum |
US20050065504A1 (en) * | 1999-07-14 | 2005-03-24 | Gerald Melsky | Guided cardiac ablation catheters |
US20060268402A1 (en) * | 2005-03-18 | 2006-11-30 | Norbert Eustergerling | Image sensor for a fluorescence scanner |
US20070087445A1 (en) * | 2005-10-14 | 2007-04-19 | The General Hospital Corporation | Arrangements and methods for facilitating photoluminescence imaging |
US20080306337A1 (en) * | 2007-06-11 | 2008-12-11 | Board Of Regents, The University Of Texas System | Characterization of a Near-Infrared Laparoscopic Hyperspectral Imaging System for Minimally Invasive Surgery |
US20090093807A1 (en) * | 2007-10-03 | 2009-04-09 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware | Vasculature and lymphatic system imaging and ablation |
US20090299354A1 (en) * | 1999-07-14 | 2009-12-03 | Cardiofocus, Inc. | Cardiac ablation catheters for forming overlapping lesions |
US20090326320A1 (en) * | 1999-07-14 | 2009-12-31 | Cardiofocus, Inc. | System and method for visualizing tissue during ablation procedures |
US20110082450A1 (en) * | 2009-10-02 | 2011-04-07 | Cardiofocus, Inc. | Cardiac ablation system with inflatable member having multiple inflation settings |
US20110082449A1 (en) * | 2009-10-02 | 2011-04-07 | Cardiofocus, Inc. | Cardiac ablation system with pulsed aiming light |
US20110082451A1 (en) * | 2009-10-06 | 2011-04-07 | Cardiofocus, Inc. | Cardiac ablation image analysis system and process |
US20110082452A1 (en) * | 2009-10-02 | 2011-04-07 | Cardiofocus, Inc. | Cardiac ablation system with automatic safety shut-off feature |
US20110158914A1 (en) * | 2009-12-25 | 2011-06-30 | Fujifilm Corporation | Fluorescence image capturing method and apparatus |
US20130324797A1 (en) * | 2012-03-30 | 2013-12-05 | Olympus Corporation | Endoscope apparatus |
US20150182118A1 (en) * | 2013-12-31 | 2015-07-02 | Memorial Sloan Kettering Cancer Center | Systems, methods, and apparatus for multichannel imaging of fluorescent sources in real time |
US20160030022A1 (en) * | 2014-07-31 | 2016-02-04 | The General Hospital Corporation | Optical Biopsy Needle and Endoscope System |
Family Cites Families (233)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3417745A (en) | 1963-08-23 | 1968-12-24 | Sheldon Edward Emanuel | Fiber endoscope provided with focusing means and electroluminescent means |
US3821510A (en) | 1973-02-22 | 1974-06-28 | H Muncheryan | Hand held laser instrumentation device |
GB1485908A (en) | 1974-05-21 | 1977-09-14 | Nath G | Apparatus for applying light radiation |
US4273109A (en) | 1976-07-06 | 1981-06-16 | Cavitron Corporation | Fiber optic light delivery apparatus and medical instrument utilizing same |
US4224929A (en) | 1977-11-08 | 1980-09-30 | Olympus Optical Co., Ltd. | Endoscope with expansible cuff member and operation section |
US4445892A (en) | 1982-05-06 | 1984-05-01 | Laserscope, Inc. | Dual balloon catheter device |
NZ205144A (en) | 1982-08-26 | 1987-03-06 | Kei Mori | Light guide with diffusing strip |
USRE34544E (en) | 1982-11-23 | 1994-02-15 | The Beth Israel Hospital Association | Method of treatment of artherosclerosis and balloon catheter the same |
US4701166A (en) | 1983-05-03 | 1987-10-20 | Catheter Technology Corp. | Valved two-way catheter |
JPS6131142A (en) | 1984-07-25 | 1986-02-13 | 富士写真光機株式会社 | Blood vessel anastomosis laser probe |
US5188632A (en) | 1984-12-07 | 1993-02-23 | Advanced Interventional Systems, Inc. | Guidance and delivery system for high-energy pulsed laser light |
US4718417A (en) | 1985-03-22 | 1988-01-12 | Massachusetts Institute Of Technology | Visible fluorescence spectral diagnostic for laser angiosurgery |
US5693043A (en) | 1985-03-22 | 1997-12-02 | Massachusetts Institute Of Technology | Catheter for laser angiosurgery |
US5318024A (en) | 1985-03-22 | 1994-06-07 | Massachusetts Institute Of Technology | Laser endoscope for spectroscopic imaging |
US5104392A (en) | 1985-03-22 | 1992-04-14 | Massachusetts Institute Of Technology | Laser spectro-optic imaging for diagnosis and treatment of diseased tissue |
US4913142A (en) | 1985-03-22 | 1990-04-03 | Massachusetts Institute Of Technology | Catheter for laser angiosurgery |
US4660925A (en) | 1985-04-29 | 1987-04-28 | Laser Therapeutics, Inc. | Apparatus for producing a cylindrical pattern of light and method of manufacture |
US4862886A (en) | 1985-05-08 | 1989-09-05 | Summit Technology Inc. | Laser angioplasty |
US4917084A (en) | 1985-07-31 | 1990-04-17 | C. R. Bard, Inc. | Infrared laser catheter system |
EP0214712B1 (en) | 1985-07-31 | 1992-09-02 | C.R. Bard, Inc. | Infrared laser catheter apparatus |
US4819632A (en) | 1986-05-19 | 1989-04-11 | Davies David H | Retrolasing catheter and method |
US4860743A (en) | 1986-10-27 | 1989-08-29 | University Of Florida | Laser method and apparatus for the recanalization of vessels and the treatment of other cardiac conditions |
US4961738A (en) | 1987-01-28 | 1990-10-09 | Mackin Robert A | Angioplasty catheter with illumination and visualization within angioplasty balloon |
US5090959A (en) | 1987-04-30 | 1992-02-25 | Advanced Cardiovascular Systems, Inc. | Imaging balloon dilatation catheter |
DE3878485D1 (en) | 1987-05-25 | 1993-03-25 | Deutsche Aerospace | DEVICE FOR CIRCUMFERENTIAL RADIATION OF OBJECTS. |
DE3750879T2 (en) | 1987-05-26 | 1995-05-11 | Surgical Laser Tech | Laser probe with a wide beam angle for contacting or insertion. |
US4770653A (en) | 1987-06-25 | 1988-09-13 | Medilase, Inc. | Laser angioplasty |
IT1220172B (en) | 1987-07-17 | 1990-06-06 | Il Consiglio Nazionale Delle R | FIBER OPTIC DEVICE FOR THE TRANSMISSION AND LATERAL IRRADIATION OF LASER ENERGY, PARTICULARLY FOR ANGIOPLASTIC TREATMENTS |
US4781681A (en) | 1987-09-15 | 1988-11-01 | Gv Medical, Inc. | Inflatable tip for laser catheterization |
US4878492A (en) | 1987-10-08 | 1989-11-07 | C. R. Bard, Inc. | Laser balloon catheter |
US4852567A (en) | 1988-01-21 | 1989-08-01 | C. R. Bard, Inc. | Laser tipped catheter |
US5026367A (en) | 1988-03-18 | 1991-06-25 | Cardiovascular Laser Systems, Inc. | Laser angioplasty catheter and a method for use thereof |
US5242437A (en) | 1988-06-10 | 1993-09-07 | Trimedyne Laser Systems, Inc. | Medical device applying localized high intensity light and heat, particularly for destruction of the endometrium |
US5125925A (en) | 1988-08-03 | 1992-06-30 | Photoradiation Systems | Intracavity laser catheter with sensing fiber |
US6066130A (en) | 1988-10-24 | 2000-05-23 | The General Hospital Corporation | Delivering laser energy |
US5140987A (en) | 1989-03-17 | 1992-08-25 | Wayne State University | Method for transvenous ablation of cardiac electrically conductive tissue by laser photocoagulation |
JP2882814B2 (en) | 1989-08-24 | 1999-04-12 | 株式会社エス・エル・ティ・ジャパン | Laser irradiation equipment |
JP3069108B2 (en) | 1989-09-01 | 2000-07-24 | 株式会社エス・エル・ティ・ジャパン | Laser light emitting device |
US5109859A (en) | 1989-10-04 | 1992-05-05 | Beth Israel Hospital Association | Ultrasound guided laser angioplasty |
US5078681A (en) | 1989-10-23 | 1992-01-07 | Olympus Optical Co., Ltd. | Balloon catheter apparatus with releasable distal seal and method of operation |
US5207699A (en) | 1989-10-30 | 1993-05-04 | Coe Frederick L | Lancet handling and disposal assembly |
US5030201A (en) | 1989-11-24 | 1991-07-09 | Aubrey Palestrant | Expandable atherectomy catheter device |
DE59006608D1 (en) | 1990-01-09 | 1994-09-01 | Ciba Geigy Ag | Light diffuser for photodynamic therapy of tumors in a patient's esophagus. |
DE59008307D1 (en) | 1990-01-09 | 1995-03-02 | Ciba Geigy Ag | Device for irradiating the bronchi of a patient for photodynamic therapy. |
US5261904A (en) | 1990-01-30 | 1993-11-16 | C. R. Bard, Inc. | Laser catheter having diffraction grating for beam shaping |
US5133709A (en) | 1990-02-23 | 1992-07-28 | Prince Martin R | Optical fiber with atraumatic rounded end for use in laser angioplasty |
US5071417A (en) | 1990-06-15 | 1991-12-10 | Rare Earth Medical Lasers, Inc. | Laser fusion of biological materials |
US5725522A (en) | 1990-06-15 | 1998-03-10 | Rare Earth Medical, Inc. | Laser suturing of biological materials |
US5188634A (en) | 1990-07-13 | 1993-02-23 | Trimedyne, Inc. | Rotatable laser probe with beveled tip |
US5053033A (en) | 1990-10-10 | 1991-10-01 | Boston Advanced Technologies, Inc. | Inhibition of restenosis by ultraviolet radiation |
US5269777A (en) | 1990-11-01 | 1993-12-14 | Pdt Systems, Inc. | Diffusion tip for optical fibers |
US5380316A (en) | 1990-12-18 | 1995-01-10 | Advanced Cardiovascular Systems, Inc. | Method for intra-operative myocardial device revascularization |
DE9116216U1 (en) | 1990-12-19 | 1992-05-27 | Fa. Carl Zeiss, 7920 Heidenheim, De | |
US5531664A (en) | 1990-12-26 | 1996-07-02 | Olympus Optical Co., Ltd. | Bending actuator having a coil sheath with a fixed distal end and a free proximal end |
JP3041099B2 (en) | 1991-02-01 | 2000-05-15 | オリンパス光学工業株式会社 | Electronic endoscope device |
US5163935A (en) | 1991-02-20 | 1992-11-17 | Reliant Laser Corporation | Surgical laser endoscopic focusing guide with an optical fiber link |
US5151096A (en) | 1991-03-28 | 1992-09-29 | Angiolaz, Incorporated | Laser catheter diffuser |
WO1992017243A2 (en) | 1991-04-05 | 1992-10-15 | Indigo Medical, Incorporated | Apparatus using a laser lucent needle |
US5190538A (en) | 1991-04-22 | 1993-03-02 | Trimedyne, Inc. | Method and apparatus for subjecting a body site to a movable beam of laterally directed laser radiation |
US5242438A (en) | 1991-04-22 | 1993-09-07 | Trimedyne, Inc. | Method and apparatus for treating a body site with laterally directed laser radiation |
US5169395A (en) | 1991-04-26 | 1992-12-08 | Pdt Cardiovascular, Inc. | Laser delivery system |
US5968039A (en) | 1991-10-03 | 1999-10-19 | Essential Dental Systems, Inc. | Laser device for performing canal surgery in narrow channels |
US5605162A (en) | 1991-10-15 | 1997-02-25 | Advanced Cardiovascular Systems, Inc. | Method for using a variable stiffness guidewire |
US5196005A (en) | 1991-11-26 | 1993-03-23 | Pdt Systems, Inc. | Continuous gradient cylindrical diffusion tip for optical fibers and method for making |
US5437660A (en) | 1991-12-30 | 1995-08-01 | Trimedyne, Inc. | Tissue ablation and a lateral-lasing fiber optic device therefor |
US5395362A (en) | 1992-01-14 | 1995-03-07 | Summit Technology | Methods and apparatus for distributing laser radiation |
WO1993015676A1 (en) | 1992-02-05 | 1993-08-19 | Angelase, Inc. | Laser catheter with movable integral fixation wire |
US5830209A (en) | 1992-02-05 | 1998-11-03 | Angeion Corporation | Multi-fiber laser catheter |
DE4237286A1 (en) | 1992-04-06 | 1994-05-05 | Laser Medizin Zentrum Ggmbh Be | Method and device for increasing the efficiency of an optical work shaft for photo-thermotherapy |
JPH05307139A (en) | 1992-04-28 | 1993-11-19 | Olympus Optical Co Ltd | Endoscope objective |
US5324284A (en) | 1992-06-05 | 1994-06-28 | Cardiac Pathways, Inc. | Endocardial mapping and ablation system utilizing a separately controlled ablation catheter and method |
EP0644742B1 (en) | 1992-06-12 | 1999-12-08 | Miravant Systems, Inc. | Diffusor tip for an optical fiber |
US5772590A (en) | 1992-06-30 | 1998-06-30 | Cordis Webster, Inc. | Cardiovascular catheter with laterally stable basket-shaped electrode array with puller wire |
US5782239A (en) | 1992-06-30 | 1998-07-21 | Cordis Webster, Inc. | Unique electrode configurations for cardiovascular electrode catheter with built-in deflection method and central puller wire |
US5292320A (en) | 1992-07-06 | 1994-03-08 | Ceramoptec, Inc. | Radial medical laser delivery device |
US6086581A (en) | 1992-09-29 | 2000-07-11 | Ep Technologies, Inc. | Large surface cardiac ablation catheter that assumes a low profile during introduction into the heart |
US5700243A (en) | 1992-10-30 | 1997-12-23 | Pdt Systems, Inc. | Balloon perfusion catheter |
US5368564A (en) | 1992-12-23 | 1994-11-29 | Angeion Corporation | Steerable catheter |
IT1266217B1 (en) | 1993-01-18 | 1996-12-27 | Xtrode Srl | ELECTROCATHETER FOR MAPPING AND INTERVENTION ON HEART CAVITIES. |
US5417653A (en) | 1993-01-21 | 1995-05-23 | Sahota; Harvinder | Method for minimizing restenosis |
US5337381A (en) | 1993-01-21 | 1994-08-09 | Fiberguide Industries | Fiber optic cylindrical diffuser |
US5409483A (en) | 1993-01-22 | 1995-04-25 | Jeffrey H. Reese | Direct visualization surgical probe |
US6161543A (en) * | 1993-02-22 | 2000-12-19 | Epicor, Inc. | Methods of epicardial ablation for creating a lesion around the pulmonary veins |
US5350375A (en) | 1993-03-15 | 1994-09-27 | Yale University | Methods for laser induced fluorescence intensity feedback control during laser angioplasty |
US5344419A (en) | 1993-04-23 | 1994-09-06 | Wayne State University | Apparatus and method for making a diffusing tip in a balloon catheter system |
JPH08509642A (en) | 1993-04-28 | 1996-10-15 | フォーカル,インコーポレイテッド | Device and method for intraluminal photothermoforming |
DE4403134A1 (en) | 1993-05-14 | 1995-08-03 | Laser Medizin Zentrum Ggmbh Be | Combination device for thermal obliteration of biological tissue |
WO1995001751A1 (en) | 1993-07-01 | 1995-01-19 | Boston Scientific Corporation | Imaging, electrical potential sensing, and ablation catheters |
US5860974A (en) | 1993-07-01 | 1999-01-19 | Boston Scientific Corporation | Heart ablation catheter with expandable electrode and method of coupling energy to an electrode on a catheter shaft |
US5630837A (en) | 1993-07-01 | 1997-05-20 | Boston Scientific Corporation | Acoustic ablation |
US5445608A (en) | 1993-08-16 | 1995-08-29 | James C. Chen | Method and apparatus for providing light-activated therapy |
US5807395A (en) | 1993-08-27 | 1998-09-15 | Medtronic, Inc. | Method and apparatus for RF ablation and hyperthermia |
US5464404A (en) | 1993-09-20 | 1995-11-07 | Abela Laser Systems, Inc. | Cardiac ablation catheters and method |
US5545209A (en) | 1993-09-30 | 1996-08-13 | Texas Petrodet, Inc. | Controlled deployment of a medical device |
US6146379A (en) | 1993-10-15 | 2000-11-14 | Ep Technologies, Inc. | Systems and methods for creating curvilinear lesions in body tissue |
US5575766A (en) | 1993-11-03 | 1996-11-19 | Daig Corporation | Process for the nonsurgical mapping and treatment of atrial arrhythmia using catheters guided by shaped guiding introducers |
US5497774A (en) | 1993-11-03 | 1996-03-12 | Daig Corporation | Guiding introducer for left atrium |
US5427119A (en) | 1993-11-03 | 1995-06-27 | Daig Corporation | Guiding introducer for right atrium |
US5363458A (en) | 1994-02-28 | 1994-11-08 | Fiber Guide Industries | Fiber optic light diffuser |
PT676218E (en) | 1994-03-25 | 2002-10-31 | Novartis Ag | LIGHT DIFFUSER AND PROCESS FOR MANUFACTURING A LIGHT DIFFUSER |
US6056744A (en) | 1994-06-24 | 2000-05-02 | Conway Stuart Medical, Inc. | Sphincter treatment apparatus |
US5680860A (en) | 1994-07-07 | 1997-10-28 | Cardiac Pathways Corporation | Mapping and/or ablation catheter with coilable distal extremity and method for using same |
US6090084A (en) | 1994-07-08 | 2000-07-18 | Daig Corporation | Shaped guiding introducers for use with a catheter for the treatment of atrial arrhythmia |
US5690611A (en) | 1994-07-08 | 1997-11-25 | Daig Corporation | Process for the treatment of atrial arrhythima using a catheter guided by shaped giding introducers |
US5431647A (en) | 1994-07-13 | 1995-07-11 | Pioneer Optics Company | Fiberoptic cylindrical diffuser |
US5441497A (en) | 1994-07-14 | 1995-08-15 | Pdt Cardiovascular, Inc. | Light diffusing guidewire |
DE9411754U1 (en) | 1994-07-20 | 1994-11-10 | Goebel Dieter Dr | Laser awl for the treatment of osteochondritis deformans |
US6572609B1 (en) | 1999-07-14 | 2003-06-03 | Cardiofocus, Inc. | Phototherapeutic waveguide apparatus |
US6270492B1 (en) | 1994-09-09 | 2001-08-07 | Cardiofocus, Inc. | Phototherapeutic apparatus with diffusive tip assembly |
US5947959A (en) | 1994-09-09 | 1999-09-07 | Rare Earth Medical, Inc. | Phototherapeutic apparatus with diffusive tip assembly |
US6558375B1 (en) | 2000-07-14 | 2003-05-06 | Cardiofocus, Inc. | Cardiac ablation instrument |
US6423055B1 (en) | 1999-07-14 | 2002-07-23 | Cardiofocus, Inc. | Phototherapeutic wave guide apparatus |
US5908415A (en) | 1994-09-09 | 1999-06-01 | Rare Earth Medical, Inc. | Phototherapy methods and apparatus |
US6676656B2 (en) | 1994-09-09 | 2004-01-13 | Cardiofocus, Inc. | Surgical ablation with radiant energy |
US8025661B2 (en) | 1994-09-09 | 2011-09-27 | Cardiofocus, Inc. | Coaxial catheter instruments for ablation with radiant energy |
US5643253A (en) | 1995-06-06 | 1997-07-01 | Rare Earth Medical, Inc. | Phototherapy apparatus with integral stopper device |
US6102905A (en) | 1994-09-09 | 2000-08-15 | Cardiofocus, Inc. | Phototherapy device including housing for an optical element and method of making |
US6579285B2 (en) | 1994-09-09 | 2003-06-17 | Cardiofocus, Inc. | Photoablation with infrared radiation |
CN1072971C (en) | 1994-09-09 | 2001-10-17 | 卡迪奥福克斯有限公司 | Phototherapeutic apparatus |
US5885278A (en) | 1994-10-07 | 1999-03-23 | E.P. Technologies, Inc. | Structures for deploying movable electrode elements |
US5722401A (en) | 1994-10-19 | 1998-03-03 | Cardiac Pathways Corporation | Endocardial mapping and/or ablation catheter probe |
US5613965A (en) | 1994-12-08 | 1997-03-25 | Summit Technology Inc. | Corneal reprofiling using an annular beam of ablative radiation |
US5715832A (en) | 1995-02-28 | 1998-02-10 | Boston Scientific Corporation | Deflectable biopsy catheter |
WO1996034646A1 (en) | 1995-05-01 | 1996-11-07 | Medtronic Cardiorhythm | Dual curve ablation catheter and method |
US5702438A (en) | 1995-06-08 | 1997-12-30 | Avitall; Boaz | Expandable recording and ablation catheter system |
EP0835075A4 (en) | 1995-06-30 | 1999-06-23 | Boston Scient Corp | Ultrasound imaging catheter with a cutting element |
US5678550A (en) * | 1995-08-11 | 1997-10-21 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Apparatus and method for in situ detection of areas of cardiac electrical activity |
US5824005A (en) | 1995-08-22 | 1998-10-20 | Board Of Regents, The University Of Texas System | Maneuverable electrophysiology catheter for percutaneous or intraoperative ablation of cardiac arrhythmias |
US5823955A (en) | 1995-11-20 | 1998-10-20 | Medtronic Cardiorhythm | Atrioventricular valve tissue ablation catheter and method |
KR0166937B1 (en) | 1995-12-29 | 1999-02-01 | 구자홍 | Shg device |
US5925038A (en) | 1996-01-19 | 1999-07-20 | Ep Technologies, Inc. | Expandable-collapsible electrode structures for capacitive coupling to tissue |
US5769843A (en) | 1996-02-20 | 1998-06-23 | Cormedica | Percutaneous endomyocardial revascularization |
US5800482A (en) | 1996-03-06 | 1998-09-01 | Cardiac Pathways Corporation | Apparatus and method for linear lesion ablation |
US5891133A (en) | 1996-03-29 | 1999-04-06 | Eclipse Surgical Technologies, Inc. | Apparatus for laser-assisted intra-coronary transmyocardial revascularization and other applications |
US6458096B1 (en) | 1996-04-01 | 2002-10-01 | Medtronic, Inc. | Catheter with autoinflating, autoregulating balloon |
US6126682A (en) | 1996-08-13 | 2000-10-03 | Oratec Interventions, Inc. | Method for treating annular fissures in intervertebral discs |
US5833682A (en) | 1996-08-26 | 1998-11-10 | Illumenex Corporation | Light delivery system with blood flushing capability |
US5891134A (en) | 1996-09-24 | 1999-04-06 | Goble; Colin | System and method for applying thermal energy to tissue |
US5931834A (en) | 1996-10-15 | 1999-08-03 | Eclipse Surgical Technologies, Inc. | Method for non-synchronous laser-assisted myocardial revascularization |
US5741249A (en) | 1996-10-16 | 1998-04-21 | Fidus Medical Technology Corporation | Anchoring tip assembly for microwave ablation catheter |
US6237605B1 (en) | 1996-10-22 | 2001-05-29 | Epicor, Inc. | Methods of epicardial ablation |
US6311692B1 (en) | 1996-10-22 | 2001-11-06 | Epicor, Inc. | Apparatus and method for diagnosis and therapy of electrophysiological disease |
US5904651A (en) | 1996-10-28 | 1999-05-18 | Ep Technologies, Inc. | Systems and methods for visualizing tissue during diagnostic or therapeutic procedures |
US6071279A (en) | 1996-12-19 | 2000-06-06 | Ep Technologies, Inc. | Branched structures for supporting multiple electrode elements |
US6012457A (en) | 1997-07-08 | 2000-01-11 | The Regents Of The University Of California | Device and method for forming a circumferential conduction block in a pulmonary vein |
US5971983A (en) | 1997-05-09 | 1999-10-26 | The Regents Of The University Of California | Tissue ablation device and method of use |
US6024740A (en) | 1997-07-08 | 2000-02-15 | The Regents Of The University Of California | Circumferential ablation device assembly |
US6251109B1 (en) | 1997-06-27 | 2001-06-26 | Daig Corporation | Process and device for the treatment of atrial arrhythmia |
US5938660A (en) | 1997-06-27 | 1999-08-17 | Daig Corporation | Process and device for the treatment of atrial arrhythmia |
US6164283A (en) * | 1997-07-08 | 2000-12-26 | The Regents Of The University Of California | Device and method for forming a circumferential conduction block in a pulmonary vein |
US6514249B1 (en) | 1997-07-08 | 2003-02-04 | Atrionix, Inc. | Positioning system and method for orienting an ablation element within a pulmonary vein ostium |
US6117101A (en) | 1997-07-08 | 2000-09-12 | The Regents Of The University Of California | Circumferential ablation device assembly |
US6652515B1 (en) | 1997-07-08 | 2003-11-25 | Atrionix, Inc. | Tissue ablation device assembly and method for electrically isolating a pulmonary vein ostium from an atrial wall |
US6245064B1 (en) * | 1997-07-08 | 2001-06-12 | Atrionix, Inc. | Circumferential ablation device assembly |
US6500174B1 (en) | 1997-07-08 | 2002-12-31 | Atrionix, Inc. | Circumferential ablation device assembly and methods of use and manufacture providing an ablative circumferential band along an expandable member |
US6117071A (en) | 1997-07-29 | 2000-09-12 | Asahi Kogaku Kogyo Kabushiki Kaisha | Endoscope with movable imaging unit for zooming or focusing |
US6554794B1 (en) | 1997-09-24 | 2003-04-29 | Richard L. Mueller | Non-deforming deflectable multi-lumen catheter |
US5995875A (en) | 1997-10-01 | 1999-11-30 | United States Surgical | Apparatus for thermal treatment of tissue |
US6217510B1 (en) | 1997-10-02 | 2001-04-17 | Olympus Optical Co., Ltd. | Endoscopes and endoscope devices which image regular observation images and fluorescent images as well as which provide easier operation of treatment tools |
US6071281A (en) | 1998-05-05 | 2000-06-06 | Ep Technologies, Inc. | Surgical method and apparatus for positioning a diagnostic or therapeutic element within the body and remote power control unit for use with same |
US6120496A (en) | 1998-05-05 | 2000-09-19 | Scimed Life Systems, Inc. | Surgical method and apparatus for positioning a diagnostic or therapeutic element within the body and coupling device for use with same |
JP2003521261A (en) | 1997-12-22 | 2003-07-15 | マイクルス コーポレイション | Variable rigidity optical fiber shaft |
US6251092B1 (en) | 1997-12-30 | 2001-06-26 | Medtronic, Inc. | Deflectable guiding catheter |
US6071302A (en) | 1997-12-31 | 2000-06-06 | Cardiofocus, Inc. | Phototherapeutic apparatus for wide-angle diffusion |
US6423058B1 (en) | 1998-02-19 | 2002-07-23 | Curon Medical, Inc. | Assemblies to visualize and treat sphincters and adjoining tissue regions |
US6064902A (en) | 1998-04-16 | 2000-05-16 | C.R. Bard, Inc. | Pulmonary vein ablation catheter |
US6562020B1 (en) | 1998-07-15 | 2003-05-13 | Corazon Technologies, Inc. | Kits for use in the treatment of vascular calcified lesions |
US6106515A (en) | 1998-08-13 | 2000-08-22 | Intraluminal Therapeutics, Inc. | Expandable laser catheter |
US6394949B1 (en) | 1998-10-05 | 2002-05-28 | Scimed Life Systems, Inc. | Large area thermal ablation |
US6245062B1 (en) | 1998-10-23 | 2001-06-12 | Afx, Inc. | Directional reflector shield assembly for a microwave ablation instrument |
US6352531B1 (en) | 1999-03-24 | 2002-03-05 | Micrus Corporation | Variable stiffness optical fiber shaft |
US6325797B1 (en) | 1999-04-05 | 2001-12-04 | Medtronic, Inc. | Ablation catheter and method for isolating a pulmonary vein |
ATE353001T1 (en) | 1999-05-11 | 2007-02-15 | Atrionix Inc | BALLOON ANCHORING WIRE |
US7935108B2 (en) | 1999-07-14 | 2011-05-03 | Cardiofocus, Inc. | Deflectable sheath catheters |
US20050222558A1 (en) | 1999-07-14 | 2005-10-06 | Cardiofocus, Inc. | Methods of cardiac ablation employing a deflectable sheath catheter |
US20050234436A1 (en) | 1999-07-14 | 2005-10-20 | Cardiofocus, Inc. | Methods of cardiac ablation in the vicinity of the right inferior pulmonary vein |
US20050234437A1 (en) | 1999-07-14 | 2005-10-20 | Cardiofocus, Inc. | Deflectable sheath catheters with out-of-plane bent tip |
DE60025087D1 (en) | 1999-07-30 | 2006-02-02 | Terumo Corp | Laser irradiation apparatus |
WO2001013812A1 (en) | 1999-08-25 | 2001-03-01 | Cardiofocus, Inc. | Maneuverable optical fiber device for cardiac photoablation |
US6702780B1 (en) | 1999-09-08 | 2004-03-09 | Super Dimension Ltd. | Steering configuration for catheter with rigid distal device |
FR2798371B1 (en) | 1999-09-10 | 2001-11-23 | Acemo | DEVICE FOR PROVIDING THE TRANSFER OF MATERIALS FROM A DEPRESSED PART TO AN OVERPRESSED PART OF A PNEUMATIC CONVEYOR |
US6579279B1 (en) | 1999-09-24 | 2003-06-17 | Omnisonics Medical Technologies, Inc. | Steerable catheter device |
US6669655B1 (en) | 1999-10-20 | 2003-12-30 | Transurgical, Inc. | Sonic element and catheter incorporating same |
WO2001035846A1 (en) | 1999-11-16 | 2001-05-25 | Ganz Robert A | System and method of treating abnormal tissue in the human esophagus |
US20010030107A1 (en) | 2000-01-03 | 2001-10-18 | Peter Simpson | Auger lock |
AU2001239964A1 (en) | 2000-02-29 | 2001-09-12 | Johns Hopkins University | Circumferential pulmonary vein ablation using a laser and fiberoptic balloon catheter |
WO2001072373A2 (en) | 2000-03-24 | 2001-10-04 | Transurgical, Inc. | Apparatus and method for intrabody thermal treatment |
US6582536B2 (en) | 2000-04-24 | 2003-06-24 | Biotran Corporation Inc. | Process for producing steerable sheath catheters |
US20020107514A1 (en) | 2000-04-27 | 2002-08-08 | Hooven Michael D. | Transmural ablation device with parallel jaws |
US6546935B2 (en) | 2000-04-27 | 2003-04-15 | Atricure, Inc. | Method for transmural ablation |
EP1642544B1 (en) | 2000-05-03 | 2009-04-08 | C.R.Bard, Inc. | Apparatus for mapping and ablation in electrophysiology procedures |
US6579278B1 (en) | 2000-05-05 | 2003-06-17 | Scimed Life Systems, Inc. | Bi-directional steerable catheter with asymmetric fulcrum |
US6375654B1 (en) | 2000-05-19 | 2002-04-23 | Cardiofocus, Inc. | Catheter system with working portion radially expandable upon rotation |
DE60109444T2 (en) | 2000-06-13 | 2006-04-13 | Atrionix, Inc., Irwindale | SURGICAL ABLATION PROBE FOR FORMING A RINGED LESION |
EP1299035B1 (en) | 2000-07-13 | 2013-02-13 | ReCor Medical, Inc. | Thermal treatment apparatus with focussed energy application |
US6796972B1 (en) | 2000-07-14 | 2004-09-28 | Edwards Lifesciences Llc | Catheter anchoring balloon structure with irrigation |
US6605055B1 (en) | 2000-09-13 | 2003-08-12 | Cardiofocus, Inc. | Balloon catheter with irrigation sheath |
US6916306B1 (en) | 2000-11-10 | 2005-07-12 | Boston Scientific Scimed, Inc. | Steerable loop structures for supporting diagnostic and therapeutic elements in contact with body tissue |
US6522933B2 (en) | 2001-03-30 | 2003-02-18 | Biosense, Webster, Inc. | Steerable catheter with a control handle having a pulley mechanism |
DE10116056B4 (en) | 2001-03-30 | 2005-09-08 | Karl Storz Gmbh & Co. Kg | Endoscopic visualization device with different image systems |
US20020183739A1 (en) | 2001-03-30 | 2002-12-05 | Long Gary L. | Endoscopic ablation system with sealed sheath |
WO2002085192A2 (en) | 2001-04-23 | 2002-10-31 | Transurgical, Inc. | Improvements in ablation therapy |
US6648875B2 (en) | 2001-05-04 | 2003-11-18 | Cardiac Pacemakers, Inc. | Means for maintaining tension on a steering tendon in a steerable catheter |
US6771996B2 (en) | 2001-05-24 | 2004-08-03 | Cardiac Pacemakers, Inc. | Ablation and high-resolution mapping catheter system for pulmonary vein foci elimination |
US6706004B2 (en) | 2001-05-31 | 2004-03-16 | Infraredx, Inc. | Balloon catheter |
US6907298B2 (en) | 2002-01-09 | 2005-06-14 | Medtronic, Inc. | Method and apparatus for imparting curves in implantable elongated medical instruments |
JP2003210028A (en) | 2002-01-23 | 2003-07-29 | Iseki & Co Ltd | Conveying screw of zoom auger |
US7717899B2 (en) | 2002-01-28 | 2010-05-18 | Cardiac Pacemakers, Inc. | Inner and outer telescoping catheter delivery system |
US6932809B2 (en) | 2002-05-14 | 2005-08-23 | Cardiofocus, Inc. | Safety shut-off device for laser surgical instruments employing blackbody emitters |
JP2004065076A (en) | 2002-08-05 | 2004-03-04 | Iseki & Co Ltd | Conveying screw of zoom auger |
US6997924B2 (en) | 2002-09-17 | 2006-02-14 | Biosense Inc. | Laser pulmonary vein isolation |
WO2004110258A2 (en) | 2003-06-10 | 2004-12-23 | Cardiofocus, Inc. | Guided cardiac ablation catheters |
US10258285B2 (en) * | 2004-05-28 | 2019-04-16 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Robotic surgical system and method for automated creation of ablation lesions |
WO2006007305A2 (en) | 2004-06-07 | 2006-01-19 | Edwards Lifesciences Corporation | Methods and devices for directionally ablating tissue |
US8137333B2 (en) * | 2005-10-25 | 2012-03-20 | Voyage Medical, Inc. | Delivery of biological compounds to ischemic and/or infarcted tissue |
US8647119B1 (en) * | 2006-04-18 | 2014-02-11 | President And Fellows Of Harvard College | Methods and kits with fluorescent probes for caries detection |
WO2007140331A2 (en) | 2006-05-25 | 2007-12-06 | Medtronic, Inc. | Methods of using high intensity focused ultrasound to form an ablated tissue area containing a plurality of lesions |
WO2008017080A2 (en) * | 2006-08-03 | 2008-02-07 | Hansen Medical, Inc. | Systems for performing minimally invasive procedures |
US11540720B2 (en) * | 2006-10-06 | 2023-01-03 | Stryker European Operations Limited | Methods, software and systems for imaging |
US20080108870A1 (en) | 2006-11-06 | 2008-05-08 | Wiita Bruce E | Apparatus and method for stabilizing an image from an endoscopic camera |
US8285367B2 (en) * | 2007-10-05 | 2012-10-09 | The Invention Science Fund I, Llc | Vasculature and lymphatic system imaging and ablation associated with a reservoir |
DK2231065T3 (en) * | 2007-12-18 | 2021-02-01 | Intersect Ent Inc | SELF-EXPANDING DEVICES |
WO2009083859A1 (en) * | 2007-12-28 | 2009-07-09 | Koninklijke Philips Electronics, N.V. | Tissue ablation device with photoacoustic lesion formation feedback |
US10219742B2 (en) * | 2008-04-14 | 2019-03-05 | Novadaq Technologies ULC | Locating and analyzing perforator flaps for plastic and reconstructive surgery |
US8241273B2 (en) * | 2009-01-09 | 2012-08-14 | Ncontact Surgical, Inc. | Method and devices for coagulation of tissue |
US8771741B2 (en) * | 2009-01-23 | 2014-07-08 | The Penn State Research Foundation | In vivo photodynamic therapy of cancer via a near infrared agent encapsulated in calcium phosphate nanoparticles |
US9254090B2 (en) * | 2010-10-22 | 2016-02-09 | Intuitive Surgical Operations, Inc. | Tissue contrast imaging systems |
EP2757933B1 (en) * | 2011-09-22 | 2019-02-06 | The George Washington University | Systems for visualizing ablated tissue |
WO2013106557A1 (en) * | 2012-01-10 | 2013-07-18 | Boston Scientific Scimed, Inc. | Electrophysiology system |
US20140350534A1 (en) * | 2013-02-20 | 2014-11-27 | Sloan-Kettering Institute For Cancer Research | Raman based ablation/resection systems and methods |
JP6635791B2 (en) * | 2013-02-20 | 2020-01-29 | スローン − ケタリング・インスティテュート・フォー・キャンサー・リサーチ | Wide-field Raman imaging apparatus and related method |
JP2017513645A (en) * | 2014-04-28 | 2017-06-01 | カーディオフォーカス,インコーポレーテッド | System and method for visualizing tissue using an ICG dye composition during an ablation procedure |
US10792087B2 (en) * | 2017-09-29 | 2020-10-06 | Biosense Webster (Israel) Ltd. | Highlighting region for re-ablation |
-
2015
- 2015-04-23 JP JP2016564561A patent/JP2017513645A/en active Pending
- 2015-04-23 EP EP15785530.5A patent/EP3137007A4/en not_active Withdrawn
- 2015-04-23 WO PCT/US2015/027314 patent/WO2015167929A1/en active Application Filing
- 2015-04-27 US US14/697,065 patent/US20150305604A1/en not_active Abandoned
-
2019
- 2019-01-28 US US16/259,483 patent/US11246476B2/en active Active
Patent Citations (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4336809A (en) * | 1980-03-17 | 1982-06-29 | Burleigh Instruments, Inc. | Human and animal tissue photoradiation system and method |
US5775327A (en) * | 1995-06-07 | 1998-07-07 | Cardima, Inc. | Guiding catheter for the coronary sinus |
US5773835A (en) * | 1996-06-07 | 1998-06-30 | Rare Earth Medical, Inc. | Fiber optic spectroscopy |
US5845646A (en) * | 1996-11-05 | 1998-12-08 | Lemelson; Jerome | System and method for treating select tissue in a living being |
US20040186351A1 (en) * | 1996-11-20 | 2004-09-23 | Olympus Optical Co., Ltd. (Now Olympus Corporation) | Fluorescent endoscope system enabling simultaneous achievement of normal light observation based on reflected light and fluorescence observation based on light with wavelengths in infrared spectrum |
US20090326320A1 (en) * | 1999-07-14 | 2009-12-31 | Cardiofocus, Inc. | System and method for visualizing tissue during ablation procedures |
US20050065504A1 (en) * | 1999-07-14 | 2005-03-24 | Gerald Melsky | Guided cardiac ablation catheters |
US20090299354A1 (en) * | 1999-07-14 | 2009-12-03 | Cardiofocus, Inc. | Cardiac ablation catheters for forming overlapping lesions |
US20020173785A1 (en) * | 2000-03-31 | 2002-11-21 | Medtronic, Inc. | System and method for positioning implantable medical devices within coronary veins |
US20020029062A1 (en) * | 2000-09-07 | 2002-03-07 | Shutaro Satake | Balloon catheter for pulmonary vein isolation |
US20030069620A1 (en) * | 2001-10-09 | 2003-04-10 | Hong Li | Balloon catheters for non-continuous lesions |
US20060268402A1 (en) * | 2005-03-18 | 2006-11-30 | Norbert Eustergerling | Image sensor for a fluorescence scanner |
US20070087445A1 (en) * | 2005-10-14 | 2007-04-19 | The General Hospital Corporation | Arrangements and methods for facilitating photoluminescence imaging |
US20080306337A1 (en) * | 2007-06-11 | 2008-12-11 | Board Of Regents, The University Of Texas System | Characterization of a Near-Infrared Laparoscopic Hyperspectral Imaging System for Minimally Invasive Surgery |
US20090093807A1 (en) * | 2007-10-03 | 2009-04-09 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware | Vasculature and lymphatic system imaging and ablation |
US20110082450A1 (en) * | 2009-10-02 | 2011-04-07 | Cardiofocus, Inc. | Cardiac ablation system with inflatable member having multiple inflation settings |
US20110082449A1 (en) * | 2009-10-02 | 2011-04-07 | Cardiofocus, Inc. | Cardiac ablation system with pulsed aiming light |
US20110082452A1 (en) * | 2009-10-02 | 2011-04-07 | Cardiofocus, Inc. | Cardiac ablation system with automatic safety shut-off feature |
US20110082451A1 (en) * | 2009-10-06 | 2011-04-07 | Cardiofocus, Inc. | Cardiac ablation image analysis system and process |
US20110158914A1 (en) * | 2009-12-25 | 2011-06-30 | Fujifilm Corporation | Fluorescence image capturing method and apparatus |
US20130324797A1 (en) * | 2012-03-30 | 2013-12-05 | Olympus Corporation | Endoscope apparatus |
US9775497B2 (en) * | 2012-03-30 | 2017-10-03 | Olympus Corporation | Endoscope apparatus for outputting signals corresponding to first and second narrowband wavelength bands |
US20150182118A1 (en) * | 2013-12-31 | 2015-07-02 | Memorial Sloan Kettering Cancer Center | Systems, methods, and apparatus for multichannel imaging of fluorescent sources in real time |
US20160030022A1 (en) * | 2014-07-31 | 2016-02-04 | The General Hospital Corporation | Optical Biopsy Needle and Endoscope System |
Cited By (85)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20200037925A1 (en) * | 2013-09-06 | 2020-02-06 | Covidien Lp | System and method for light based lung visualization |
US11246476B2 (en) * | 2014-04-28 | 2022-02-15 | Cardiofocus, Inc. | Method for visualizing tissue with an ICG dye composition during ablation procedures |
US11344365B2 (en) | 2016-01-05 | 2022-05-31 | Cardiofocus, Inc. | Ablation system with automated sweeping ablation energy element |
US11832878B2 (en) | 2016-01-05 | 2023-12-05 | Cardiofocus, Inc. | Ablation system with automated ablation energy element |
US11921275B2 (en) * | 2016-02-15 | 2024-03-05 | Leica Instruments (Singapore) Pte. Ltd. | Illumination filter system and observation system for a multispectral fluorescence microscope, multispectral fluorescence microscope, and microscopying method |
US20170235118A1 (en) * | 2016-02-15 | 2017-08-17 | Leica Instruments (Singapore) Pte. Ltd. | Illumination filter system and observation system for a multispectral fluorescence microscope, multispectral fluorescence microscope, and microscopying method |
US10823947B2 (en) * | 2016-02-15 | 2020-11-03 | Leica Instruments (Singapore) Pte. Ltd. | Illumination filter system and observation system for a multispectral fluorescence microscope, multispectral fluorescence microscope, and microscopying method |
US20210018738A1 (en) * | 2016-02-15 | 2021-01-21 | Leica Instruments (Singapore) Pte. Ltd. | Illumination filter system and observation system for a multispectral fluorescence microscope, multispectral fluorescence microscope, and microscopying method |
US20190122345A1 (en) * | 2016-04-04 | 2019-04-25 | Sony Corporation | Image processing apparatus, imaging apparatus, image processing method, and program |
US10929959B2 (en) * | 2016-04-04 | 2021-02-23 | Sony Corporation | Image processing apparatus, imaging apparatus, and image processing method |
USD851245S1 (en) | 2017-04-14 | 2019-06-11 | Cardiofocus, Inc. | Compliant balloon |
JP2019042156A (en) * | 2017-09-01 | 2019-03-22 | 富士フイルム株式会社 | Medical image processing apparatus, endoscope apparatus, diagnosis support apparatus, and medical service support apparatus |
US11900623B2 (en) | 2017-12-27 | 2024-02-13 | Cilag Gmbh International | Hyperspectral imaging with tool tracking in a light deficient environment |
EP3731725A4 (en) * | 2017-12-27 | 2021-10-13 | Ethicon LLC | Fluorescence imaging in a light deficient environment |
US11823403B2 (en) | 2017-12-27 | 2023-11-21 | Cilag Gmbh International | Fluorescence imaging in a light deficient environment |
US11574412B2 (en) | 2017-12-27 | 2023-02-07 | Cilag GmbH Intenational | Hyperspectral imaging with tool tracking in a light deficient environment |
CN111526776A (en) * | 2017-12-27 | 2020-08-11 | 爱惜康有限责任公司 | Fluorescence imaging in low light environments |
US11389236B2 (en) | 2018-01-15 | 2022-07-19 | Cardiofocus, Inc. | Ablation system with automated ablation energy element |
US11540696B2 (en) | 2019-06-20 | 2023-01-03 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed fluorescence imaging system |
US11668921B2 (en) | 2019-06-20 | 2023-06-06 | Cilag Gmbh International | Driving light emissions according to a jitter specification in a hyperspectral, fluorescence, and laser mapping imaging system |
US11284785B2 (en) | 2019-06-20 | 2022-03-29 | Cilag Gmbh International | Controlling integral energy of a laser pulse in a hyperspectral, fluorescence, and laser mapping imaging system |
US11288772B2 (en) | 2019-06-20 | 2022-03-29 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed fluorescence imaging system |
US11311183B2 (en) | 2019-06-20 | 2022-04-26 | Cilag Gmbh International | Controlling integral energy of a laser pulse in a fluorescence imaging system |
US11949974B2 (en) | 2019-06-20 | 2024-04-02 | Cilag Gmbh International | Controlling integral energy of a laser pulse in a fluorescence imaging system |
US11337596B2 (en) | 2019-06-20 | 2022-05-24 | Cilag Gmbh International | Controlling integral energy of a laser pulse in a fluorescence imaging system |
US11284784B2 (en) | 2019-06-20 | 2022-03-29 | Cilag Gmbh International | Controlling integral energy of a laser pulse in a fluorescence imaging system |
US11360028B2 (en) | 2019-06-20 | 2022-06-14 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed hyperspectral, fluorescence, and laser mapping imaging system |
US11280737B2 (en) | 2019-06-20 | 2022-03-22 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed fluorescence imaging system |
US11389066B2 (en) | 2019-06-20 | 2022-07-19 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed hyperspectral, fluorescence, and laser mapping imaging system |
US11398011B2 (en) | 2019-06-20 | 2022-07-26 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed laser mapping imaging system |
US11399717B2 (en) | 2019-06-20 | 2022-08-02 | Cilag Gmbh International | Hyperspectral and fluorescence imaging and topology laser mapping with minimal area monolithic image sensor |
US11412152B2 (en) | 2019-06-20 | 2022-08-09 | Cilag Gmbh International | Speckle removal in a pulsed hyperspectral imaging system |
US11412920B2 (en) * | 2019-06-20 | 2022-08-16 | Cilag Gmbh International | Speckle removal in a pulsed fluorescence imaging system |
US11432706B2 (en) | 2019-06-20 | 2022-09-06 | Cilag Gmbh International | Hyperspectral imaging with minimal area monolithic image sensor |
US11477390B2 (en) | 2019-06-20 | 2022-10-18 | Cilag Gmbh International | Fluorescence imaging with minimal area monolithic image sensor |
US11471055B2 (en) | 2019-06-20 | 2022-10-18 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed fluorescence imaging system |
US11940615B2 (en) | 2019-06-20 | 2024-03-26 | Cilag Gmbh International | Driving light emissions according to a jitter specification in a multispectral, fluorescence, and laser mapping imaging system |
US11516388B2 (en) | 2019-06-20 | 2022-11-29 | Cilag Gmbh International | Pulsed illumination in a fluorescence imaging system |
US11516387B2 (en) | 2019-06-20 | 2022-11-29 | Cilag Gmbh International | Image synchronization without input clock and data transmission clock in a pulsed hyperspectral, fluorescence, and laser mapping imaging system |
US11531112B2 (en) | 2019-06-20 | 2022-12-20 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a hyperspectral, fluorescence, and laser mapping imaging system |
US11533417B2 (en) | 2019-06-20 | 2022-12-20 | Cilag Gmbh International | Laser scanning and tool tracking imaging in a light deficient environment |
US11937784B2 (en) | 2019-06-20 | 2024-03-26 | Cilag Gmbh International | Fluorescence imaging in a light deficient environment |
US11550057B2 (en) | 2019-06-20 | 2023-01-10 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a fluorescence imaging system |
US11276148B2 (en) | 2019-06-20 | 2022-03-15 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed fluorescence imaging system |
US11589819B2 (en) | 2019-06-20 | 2023-02-28 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a laser mapping imaging system |
US11612309B2 (en) | 2019-06-20 | 2023-03-28 | Cilag Gmbh International | Hyperspectral videostroboscopy of vocal cords |
US11617541B2 (en) | 2019-06-20 | 2023-04-04 | Cilag Gmbh International | Optical fiber waveguide in an endoscopic system for fluorescence imaging |
US11622094B2 (en) | 2019-06-20 | 2023-04-04 | Cilag Gmbh International | Wide dynamic range using a monochrome image sensor for fluorescence imaging |
US11624830B2 (en) | 2019-06-20 | 2023-04-11 | Cilag Gmbh International | Wide dynamic range using a monochrome image sensor for laser mapping imaging |
US11633089B2 (en) | 2019-06-20 | 2023-04-25 | Cilag Gmbh International | Fluorescence imaging with minimal area monolithic image sensor |
US11668920B2 (en) | 2019-06-20 | 2023-06-06 | Cilag Gmbh International | Driving light emissions according to a jitter specification in a fluorescence imaging system |
US11284783B2 (en) | 2019-06-20 | 2022-03-29 | Cilag Gmbh International | Controlling integral energy of a laser pulse in a hyperspectral imaging system |
US11668919B2 (en) | 2019-06-20 | 2023-06-06 | Cilag Gmbh International | Driving light emissions according to a jitter specification in a laser mapping imaging system |
US11671691B2 (en) | 2019-06-20 | 2023-06-06 | Cilag Gmbh International | Image rotation in an endoscopic laser mapping imaging system |
US11674848B2 (en) | 2019-06-20 | 2023-06-13 | Cilag Gmbh International | Wide dynamic range using a monochrome image sensor for hyperspectral imaging |
US11686847B2 (en) | 2019-06-20 | 2023-06-27 | Cilag Gmbh International | Pulsed illumination in a fluorescence imaging system |
US11700995B2 (en) | 2019-06-20 | 2023-07-18 | Cilag Gmbh International | Speckle removal in a pulsed fluorescence imaging system |
US11712155B2 (en) | 2019-06-20 | 2023-08-01 | Cilag GmbH Intenational | Fluorescence videostroboscopy of vocal cords |
US11716533B2 (en) | 2019-06-20 | 2023-08-01 | Cilag Gmbh International | Image synchronization without input clock and data transmission clock in a pulsed fluorescence imaging system |
US11716543B2 (en) | 2019-06-20 | 2023-08-01 | Cilag Gmbh International | Wide dynamic range using a monochrome image sensor for fluorescence imaging |
US11727542B2 (en) | 2019-06-20 | 2023-08-15 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed hyperspectral, fluorescence, and laser mapping imaging system |
US11740448B2 (en) | 2019-06-20 | 2023-08-29 | Cilag Gmbh International | Driving light emissions according to a jitter specification in a fluorescence imaging system |
US11747479B2 (en) | 2019-06-20 | 2023-09-05 | Cilag Gmbh International | Pulsed illumination in a hyperspectral, fluorescence and laser mapping imaging system |
US11758256B2 (en) | 2019-06-20 | 2023-09-12 | Cilag Gmbh International | Fluorescence imaging in a light deficient environment |
US11754500B2 (en) | 2019-06-20 | 2023-09-12 | Cilag Gmbh International | Minimizing image sensor input/output in a pulsed fluorescence imaging system |
US11788963B2 (en) | 2019-06-20 | 2023-10-17 | Cilag Gmbh International | Minimizing image sensor input/output in a pulsed fluorescence imaging system |
US11793399B2 (en) | 2019-06-20 | 2023-10-24 | Cilag Gmbh International | Super resolution and color motion artifact correction in a pulsed hyperspectral imaging system |
US11821989B2 (en) | 2019-06-20 | 2023-11-21 | Cllag GmbH International | Hyperspectral, fluorescence, and laser mapping imaging with fixed pattern noise cancellation |
US11266304B2 (en) | 2019-06-20 | 2022-03-08 | Cilag Gmbh International | Minimizing image sensor input/output in a pulsed hyperspectral imaging system |
US11931009B2 (en) | 2019-06-20 | 2024-03-19 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a hyperspectral imaging system |
US11854175B2 (en) | 2019-06-20 | 2023-12-26 | Cilag Gmbh International | Fluorescence imaging with fixed pattern noise cancellation |
US11877065B2 (en) | 2019-06-20 | 2024-01-16 | Cilag Gmbh International | Image rotation in an endoscopic hyperspectral imaging system |
US11882352B2 (en) | 2019-06-20 | 2024-01-23 | Cllag GmbH International | Controlling integral energy of a laser pulse in a hyperspectral,fluorescence, and laser mapping imaging system |
US11892403B2 (en) | 2019-06-20 | 2024-02-06 | Cilag Gmbh International | Image synchronization without input clock and data transmission clock in a pulsed fluorescence imaging system |
US11895397B2 (en) | 2019-06-20 | 2024-02-06 | Cilag Gmbh International | Image synchronization without input clock and data transmission clock in a pulsed fluorescence imaging system |
US11925328B2 (en) | 2019-06-20 | 2024-03-12 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed hyperspectral imaging system |
US11898909B2 (en) | 2019-06-20 | 2024-02-13 | Cilag Gmbh International | Noise aware edge enhancement in a pulsed fluorescence imaging system |
US11903563B2 (en) | 2019-06-20 | 2024-02-20 | Cilag Gmbh International | Offset illumination of a scene using multiple emitters in a fluorescence imaging system |
US11924535B2 (en) | 2019-06-20 | 2024-03-05 | Cila GmbH International | Controlling integral energy of a laser pulse in a laser mapping imaging system |
CN110510147A (en) * | 2019-08-02 | 2019-11-29 | 西安飞机工业(集团)有限责任公司 | A kind of aircaft configuration crack detecting method |
WO2022031615A1 (en) * | 2020-08-06 | 2022-02-10 | Medtronic Navigation, Inc. | Tumor ablation planning using interstitial optical mapping |
US20220039744A1 (en) * | 2020-08-06 | 2022-02-10 | Medtronic Navigation, Inc. | Tumor ablation planning using interstitial optical mapping |
US20220079600A1 (en) * | 2020-09-15 | 2022-03-17 | Baylis Medical Company Inc. | Medical guidewire assembly |
US20220142708A1 (en) * | 2020-11-12 | 2022-05-12 | Cardiofocus, Inc. | Ablation Catheters with Multiple Endoscopes and Imaging Chip Endoscopes and System for Altering an Orientation of an Endoscopic Image |
WO2022212849A3 (en) * | 2021-04-01 | 2022-11-10 | Cardiofocus, Inc. | Deployable structures to provide electrodes on the surface of an endoscopically guided laser ablation catheter |
Also Published As
Publication number | Publication date |
---|---|
US20190150718A1 (en) | 2019-05-23 |
EP3137007A4 (en) | 2017-09-27 |
JP2017513645A (en) | 2017-06-01 |
US11246476B2 (en) | 2022-02-15 |
WO2015167929A1 (en) | 2015-11-05 |
EP3137007A1 (en) | 2017-03-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11246476B2 (en) | Method for visualizing tissue with an ICG dye composition during ablation procedures | |
EP2485671B1 (en) | Cardiac ablation image analysis system | |
US11457817B2 (en) | Systems and methods for hyperspectral analysis of cardiac tissue | |
JP4418234B2 (en) | Endoscope system | |
US10154888B2 (en) | System and method for visual confirmation of pulmonary vein isolation during abalation procedures | |
US9254090B2 (en) | Tissue contrast imaging systems | |
CN104066368B (en) | Systems and methods for visualizing ablated tissue | |
AU782257B2 (en) | Method and apparatus for performing intra-operative angiography | |
US5762609A (en) | Device and method for analysis of surgical tissue interventions | |
US11382515B2 (en) | Renal denervation using nerve fluorescing dye | |
US11832878B2 (en) | Ablation system with automated ablation energy element | |
US20210369118A1 (en) | Lesion visualization using dual wavelength approach |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: CARDIOFOCUS, INC., MASSACHUSETTS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:MELSKY, GERALD;REEL/FRAME:037425/0004 Effective date: 20160105 |
|
AS | Assignment |
Owner name: SOLAR CAPITAL LTD., NEW YORK Free format text: SECURITY INTEREST;ASSIGNOR:CARDIOFOCUS, INC.;REEL/FRAME:041805/0976 Effective date: 20170331 Owner name: SILICON VALLEY BANK, MASSACHUSETTS Free format text: SECURITY INTEREST;ASSIGNOR:CARDIOFOCUS, INC.;REEL/FRAME:041805/0976 Effective date: 20170331 |
|
AS | Assignment |
Owner name: GPB DEBT HOLDINGS II LLC, NEW YORK Free format text: SECURITY INTEREST;ASSIGNOR:CARDIOFOCUS, INC.;REEL/FRAME:045478/0532 Effective date: 20180404 |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: FINAL REJECTION MAILED |
|
AS | Assignment |
Owner name: CARDIOFOCUS, INC., MASSACHUSETTS Free format text: RELEASE BY SECURED PARTY;ASSIGNORS:SILICON VALLEY BANK;OXFORD FINANCE LLC;REEL/FRAME:049133/0474 Effective date: 20190509 |
|
AS | Assignment |
Owner name: CARDIOFOCUS, INC., MASSACHUSETTS Free format text: RELEASE BY SECURED PARTY;ASSIGNORS:SILICON VALLEY BANK;OXFORD FINANCE LLC;REEL/FRAME:049138/0233 Effective date: 20190509 Owner name: CARDIOFOCUS, INC., MASSACHUSETTS Free format text: RELEASE BY SECURED PARTY;ASSIGNORS:SILICON VALLEY BANK;SOLAR CAPITAL LTD.;REEL/FRAME:049138/0362 Effective date: 20190509 Owner name: KENNEDY LEWIS INVESTMENT MANAGEMENT LLC, NEW YORK Free format text: INTELLECTUAL PROPERTY SECURITY AGREEMENT;ASSIGNOR:CARDIOFOCUS, INC.;REEL/FRAME:049149/0356 Effective date: 20190510 |
|
AS | Assignment |
Owner name: CARDIOFOCUS, INC., MASSACHUSETTS Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:GPB DEBT HOLDINGS II, LLC;REEL/FRAME:049200/0597 Effective date: 20190510 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |