Biosense Webster (israel) Ltd.

Johnson & Johnson Surgical Vision, Inc.

Acclarent, Inc.

Other

Biosense Webster (isreal) Ltd.

Biosense Webster, Inc.

Vadim Gliner

Assaf Govari

Andres Claudio Altmann

Ilya Sitnitsky

Yehuda Algawi

Alon Boumendil

Yair Palti

Christopher Thomas Beeckler

Yaron Ephrath

Ram Bernard Mayer

Remi Bettan

Jetmir Palushi

Israel Zilberman

Joseph Thomas Keyes

Fatemeh Akbarian

Ehsan Shameli

Henry F Salazar

Itamar Bustan

Babak Ebrahimi

Shubhayu Basu

George L Matlock

Itzhak Fang

Akram Zoabi

John H Thinnes, Jr

Fady Massarwi

Don Q Ngo-Chu

Amit Fuchs

Zvi Dekel

Marc Dean

Moran Levi

Madison K Vanosdoll

Hany Abdelwahed

Yitzhack Schwartz

Thomas R Jenkins

Randy J Kesten

Athanassios Papaioannou

Noam Racheli

Yoav Pinsky

Eran Aharon

Athanasios Papadakis

Yael Buchnik

Uri Avni

Alexander Salevich

Ygal Zucker

Ilan Goldenberg

Alison D Wright

Shai Shimon Bard

David A Smith, Jr

Stanislav Katzir

Gili Attias

Behnam Amin

Eden Kidishman

Kevin Mark Okarski

Karthick Ramyan Mohan

Sharona Ben Shoshan

Noam Rachli

Ghislain G Sema

Dganit David

Uriel Hod

Benham Amin

Eyal Dror

Yoav Lamhot

Ahmed Albayoumy

Valerie Emparado

George Gusein

Aleksander Prylutskyy

Franklin D Tarke

Christian W Wangsgard

Yan Korgozki

Ilya Sitniksky

Ram B Mayer

John H Thinnes

Andreas Claudio Altmann

Guy Wekselman

Vladimir Dvorkin

Benjamin Cohen

Natan Sharon Katz

An eye surgery system includes an Input/Output (I/O) device and a processor. The I/O device is configured to enable a user to define one or more eye surgery protocols, and further configured to, using the I/O device, present a graphical user interface (GUI) that displays one or more user defined eye surgery protocols. The processor is configured to (a) present the one or more user defined eye surgery protocols on the I/O device using the GUI, (b) test compatibility of the one or more user defined eye surgery protocols with the eye surgery system, and (c) provide an indication of the compatibility to a user of the eye surgery system.

Managing phacoemulsification user defined protocols

A phacoemulsification system including a phacoemulsification probe having a probe body, a horn disposed at least partially in the probe body, a needle coupled with the horn and configured to be inserted into an eye, and a piezoelectric actuator disposed in the probe body and configured to vibrate the horn and the needle in a first direction with a stroke length with respect to the probe body; a signal generator configured to generate a drive signal to drive a vibration of the piezoelectric actuator; a stroke measurement apparatus configured to provide indications of the stroke length of the needle over time; and a controller configured to dynamically adjust a frequency of the drive signal so as to maximize the stroke length and maintain mechanical resonance of the needle responsively to the provided indications of the stroke length.

Phacoemulsification probe stroke length maximization system

A system and method that includes inserting a needle of a phacoemulsification handpiece into an eye of a patient and vibrating the needle in a first trajectory. Matter from the eye is aspirated via an aspiration line while the needle is vibrated in the first trajectory. An indication is received, of a vacuum level in the aspiration line. Determined is, that the vacuum level has changed by at least a preset vacuum level change, and in response vibrating the needle is switched to a second trajectory, different from the first trajectory.

Automatic control of phacoemulsification needle trajectory

An apparatus includes a body, a shaft assembly, and a visualization assembly. The body includes first and second actuators. The shaft assembly extends distally from the body and includes a rigid proximal portion and a steerable distal portion. The steerable distal portion is positioned distally relative to the rigid proximal portion. The first actuator is operable to drive the steerable distal portion to deflect laterally relative to a longitudinal axis defined by the rigid proximal portion. The steerable distal portion is configured to fit within a nasal cavity of a patient. The visualization assembly is disposed within the shaft assembly. The visualization assembly includes a camera. The second actuator is operable to drive longitudinal translation of the visualization assembly relative to the shaft assembly.

ENT instrument with deformable guide having translatable imaging feature

A system includes a display and a processor. The processor is configured to (i) receive a cardiac electrophysiological (EP) velocity vectors map, (ii) compute a set of directed graphs from at least some of the velocity vectors, (iii) using the directed graphs, identify respective origin velocity vectors on the EP velocity vectors map, (iv) define one or more regions on the EP velocity vectors map, (v) determining based on origin velocity vectors in each of the one or more regions, whether the one or more regions contain a focal source of an arrhythmia, and (vi) visualize regions identified to contain a focal source on the EP map to a user, on the display.

Focal arrhythmia source finder using directed graphs

A catheter includes: (a) a shaft for insertion into a heart of a patient, (b) an expandable distal-end assembly, which is coupled to the shaft and is configured to make contact with tissue of the heart, (c) at least first and second electrocardiogram (ECG) electrodes, which are coupled to an outer surface of the expandable distal-end assembly, and when placed in contact with the tissue, are configured to sense ECG signals in the tissue, and (d) a reference electrode, which is positioned within an inner volume of the distal-end assembly, and in an expanded position of the distal-end assembly, the reference electrode: (i) has no physical contact with the tissue, and (ii) is positioned at a first distance from the first ECG electrode and at a second distance from the second ECG electrode, and the difference between the first and second distances is smaller than a predefined threshold.

Electro-anatomical mapping and annotation presented in electrophysiological procedures

In one embodiment, a phacoemulsification system includes a phacoemulsification probe configured to be inserted into an eye, and including a needle, a horn configured to support the needle, and an ultrasonic actuator connected to the horn and configured to vibrate the needle to emulsify a lens of the eye, an aspiration line partially disposed in the needle, a pumping sub-system connected to the aspiration line and configured to remove fluid and waste matter from the eye via the aspiration line, a valve disposed in the aspiration line and configured to control fluid connectivity in the aspiration line, a sensor configured to provide a signal indicative of a fluid metric in the aspiration line, and a controller configured to find an activation status of the ultrasonic actuator, and selectively control the valve responsively to the fluid metric and the activation status of the ultrasonic actuator.

Anti-vacuum surge system

A system comprising a processor and memory storing instructions configured to cause the system to: receive multiple electrophysiological (EP) signals acquired by multiple electrodes of a multi-electrode catheter that are in contact with tissue in a region of a cardiac chamber, and respective tissue locations at which the electrodes acquired the EP signals, calculate an average local activation time, determine: a first section of two sections having a smaller average LAT value, and a second section of the two sections having a higher average value, determine a first representative location in the first section, and a second representative location in the second section, calculate a propagation vector indicative of propagation of an EP wave that has generated the EP signals, determine if a re-entering EP wave is detected, and calculate an additional propagation vector for the re-entering EP wave.

Analyzing multi-electrode catheter signals to determine electrophysiological (EP) wave propagation vector

An apparatus includes a current source, an electronic circuit and a circuit board. The current source is configured to flow an electrical current having a selected frequency between a pair of electrodes coupled to a medical probe. The electronic circuit is configured to measure a single-ended voltage relative to ground that is formed on at least one of the electrodes in the pair in response to the electrical current, and, based on the measured voltage, to assess physical contact between the at least one of the electrodes and tissue. The circuit board includes the current source and the electronic circuit, and includes a layout that produces, at the selected frequency, a predefined capacitance between the current source and ground, thus forming a reference for measurement of the single-ended voltage.

Assessing tissue contact with catheter using pairs of electrodes and common reference ground established using designed circuit-board capacitance

In one example, a medical system includes a display, a console including a plurality of ports configured to be coupled with the catheters via respective cables, the catheters having respective first electrical channel profiles, the ports having respective second electrical channel profiles, and processing circuitry configured to receive user input selecting respective ones of the catheters to be used in a medical procedure. find a connection configuration with which to couple the respective ones of the catheters with ones of the ports, responsively to the respective first electrical channel profiles of the respective ones of the catheters and the respective second electrical channel profiles of the ports, and render the connection configuration to the display.

Catheter connection configuration system

A system includes a medical instrument, a position sensor, and a processor. The medical instrument includes a handle and a head, the head being configured for insertion into an organ of a patient and having a feature that is rotationally-asymmetric about a longitudinal axis of the medical instrument. The position sensor, which is disposed on the head and is configured to generate signals in response to an externally-applied magnetic field. The processor is configured to receive the signals generated by the position sensor on the head, and estimate, based on the received signals, a roll angle of the rotationally-asymmetric feature of the head.

Finding roll angle of distal end of deflectable or non-deflectable invasive medical instrument

A method for calibrating a probe includes applying respective harmonic electrical signals having respective amplitudes and respective phases to multiple piezoelectric crystals coupled with a tip of the probe so as to cause the tip to vibrate, observing a motion of the tip while applying the respective harmonic electrical signals, adjusting the respective amplitudes and the respective phases of the signals so as to cause the observed motion of the tip to conform to a predefined trajectory, and recording an indication of the respective, adjusted amplitudes and phases in a memory contained in the probe.

Compensating for imperfect behavior of multi-piezoelectric crystal

A system includes a processor and a display. The processor is configured to: (i) produce an electroanatomic (EA) map of a surface of the organ, the EA map specifying a propagation vector-field (PVF) indicative of propagation of an electrophysiological (EP) wave over at least the surface, (ii) select at least a region of the organ, (iii) calculate a gaussian integral of the PVF along a perimeter of at least a closed contour indicative of the selected region, and (iii) produce at the region, a tag indicative of the LAS, in case the calculated gaussian integral meets a criterion. The display is configured to display the EA map and at least the tag over the EA map.

Detecting local activation source in atrial fibrillation

In one embodiment, a medical system includes a catheter configured to be inserted into a chamber of a heart of a living subject, and including catheter electrodes configured to contact tissue at respective locations within the chamber of the heart, a display, and a processing circuitry configured to receive respective signals from the catheter captured by respective ones of the electrodes, assess conformity of each of the respective signals to at least one signal characteristic, find a given one of the signals of a given one of the electrodes not conforming to the at least one signal characteristic for a given time period, and render to the display an indication that the given signal of the given electrode does not conform to the at least one signal characteristic for the given time period.

Transient event identification

A system includes a processor to receive multiple electrophysiological (EP) signals acquired by multiple electrodes of a multi-electrode catheter that are in contact with tissue in a region of a cardiac chamber, and respective tissue locations at which the electrodes acquired the EP signals. The processor calculates local activation time (LAT) values for the respective tissue locations, and compares the average LAT values to determine representative locations. Based on a comparison between average LAT values the processor produces a propagation vector indicative of a propagation of an EP wave that has generated the EP signals and displays the propagation vector to a user.

Mapping resolution of electrophysiological (EP) wave propagating on the surface of patient heart

Growing community of inventors

Haifa, Israel

Vadim Gliner