Abstract: Apparatus, including a tube having proximal and distal ends and an internal lumen. The distal end may bend up to 270°, and the tube may be inserted into an eye. A planar resilient strip, having proximal and distal ends, is inserted into the internal lumen, and the strip distal end is fixed to the tube distal end. A coil spring is fixed to the strip proximal end so that a coil spring symmetry axis is coplanar with the strip. A camera, mounted with the strip distal end, images the eye interior. A wire is fixed to the strip distal end, so that a predetermined force on the wire causes the tube distal end to bend by a preset angle. A magnetometer at the tube proximal end is configured, when a nonvarying magnetic field traverses it, to provide a signal that, when taken with the preset angle, indicates a camera orientation.

Abstract: A method that includes selectively positioning an ablation catheter system at a treatment site comprising cardiac tissue, ablating cardiac tissue at the treatment site with the ablation catheter system using a power setting of approximately 90 W applied to tissue for approximately four (4) seconds to achieve a target electrode temperature, and achieving approximately zero incidence of steam pop occurrence in both left and right atrial ablations and complete pulmonary vein isolation, by the ablation catheter system, for all patients of a predetermined patient population suffering from paroxysmal atrial fibrillation (PAF).

Abstract: A location pad includes two or more field-generators, and a frame. The field-generators are configured to generate respective magnetic fields at least in a region-of-interest (ROI) of a patient organ, for measuring a position of a medical instrument in the ROI. The frame is coupled with tissue that is at least partially surrounding the organ and is configured to fix the two or more field-generators at respective positions surrounding the ROI.

Abstract: A location pad includes two or more field-generators, one or more tracking elements, and a frame. The field-generators are configured to generate respective magnetic fields at least in a region-of-interest (ROI) of an organ of a patient, for measuring a position of a medical instrument in the ROI. The one or more tracking elements are for registering the location pad with the organ. The frame is coupled with tissue that is at least partially surrounding the organ, and the frame is configured to fix (i) the two or more field-generators at respective positions surrounding at least a portion of the ROI, and (ii) the one or more tracking elements at one or more respective predefined positions on the frame.

Abstract: A surgical imaging system, including a first imaging device configured to generate a real-time visual image of a first field of view of a patient, and a second imaging device configured to generate a real-time thermal image of the first field of view. The system also includes a retaining structure, configured to be positioned in proximity to an eye of an operator, and a semitransparent screen configured to be mounted on the structure. The system additionally includes a processor configured to receive the images, and upon receiving an indication from the operator, to present, on the screen, the real-time visual image, or the real-time thermal image or the real-time thermal image overlaid on the real-time visual image, focused to a point in proximity to a near point of the eye while the operator can view, through the screen, a second field of view different from the first field of view.

Abstract: In one embodiment, a system includes generator coils to generate respective magnetic fields, a catheter including a distal end, which includes magnetic coil sensors to output electrical signals based on detection of the respective magnetic fields, and processing circuitry to receive the electrical signals from the magnetic coil sensors, select at least one of magnetic fields having a magnetic field gradient as a function of at least one of the received electrical signals, compute a difference between magnetic field magnitudes of the at least one selected magnetic field detected by the first magnetic coil sensor and the second magnetic coil sensor as a function of the electrical signals, and compute a dimension of the distal end, based on the difference between the magnetic field magnitudes of the at least one selected magnetic field and the magnetic field gradient of the at least one selected magnetic field.

Abstract: A system, method and computer program product, the system comprising: a phacoemulsification probe having a needle at its distal end, the needle configured to be inserted into an eye of a patient; a pressure sensor, and a processor, configured to repeatedly: obtain a plurality of pressure values taken by the pressure sensor, each of the plurality of pressure values indicating an intraocular pressure (IOP) measurement taken during a surgical procedure; calculate an overall measurement for the surgical procedure based on the pressure values; and displaying on a display device a graphic representation of the overall measurement.

Abstract: An apparatus includes a shaft and an inflatable sleeve catheter. The shaft is configured for insertion through a sheath into a cavity of an organ of a patient. The inflatable sleeve catheter is fixed to a distal end of the shaft, with the inflatable sleeve catheter including (i) a resilient inner end section, which is fixed to the distal end of the shaft and is formed so as to assume a predefined shape when unconstrained, (ii) an inflatable sleeve that envelopes the inner end section, and a plurality of electrodes that are disposed over the inflatable sleeve and are configured to contact tissue.

Abstract: A flexible probe has an assembly in its distal end. The assembly has a distal side and a proximal side. The assembly includes first and second flat spring coils having internal edges that mate with first and second retainers, respectively. The first and second flat coils are disposed in the probe distal end proximal to the electrode and separated by a spacer. The first and second flat coils are configured to deform in response to pressure exerted on the distal tip when the tip engages a wall of the body cavity. A transmitter is disposed on one of the distal side or the proximal side of the assembly and a receiver is disposed on the opposite side. The receiver is configured to receive signals from the transmitter for sensing a position of the receiver relative to the transmitter.

Abstract: A medical system includes a catheter, a light source, a detector, a circulator, and a processor. The catheter includes a distal-end assembly for performing a medical operation on tissue in a cavity of an organ of a patient, the distal-end assembly including an optical fiber configured to guide transmitted light to interact with the tissue of the cavity, and to guide returned light that interacted with the tissue. The light source is configured to produce the transmitted light. The detector is configured to measure the returned light. The circulator is configured to couple the transmitted light from the light source to the optical fiber, and to couple the returned light from the optical fiber to the detector. The processor is configured to identify a contact of the distal-end assembly with the tissue based on the returned light measured by the detector, and to indicate the identified contact to a user.

Abstract: In one embodiment, a catheter includes a shaft assembly having a proximal and distal end, which comprises a deflectable segment including lumens running longitudinally therein, electrodes disposed at the distal end, a connector disposed at the proximal end for coupling to processing circuitry, cables disposed in first respective ones of the lumens, each cable electrically coupled to the connector and a respective group of the electrodes, wherein each cable includes a bundle of wires, each wire connected to a respective one of the electrodes in the respective group, an electrical shielding surrounding the bundle, and an electrically insulating jacket surrounding the shielding and sized to allow longitudinal movement of the respective cable within the respective lumen, respective elongated members disposed in second respective ones of the lumens, and connected to the distal end, and a manipulator connected to the elongated members to actuate the distal end via the elongated members.

Abstract: A disposable dual-action reciprocating pump part includes a piston and a cylinder, and multiple silicone O-rings. The piston is configured to move bi-directionally inside the cylinder. The multiple silicone O-rings are configured to seal the piston against the cylinder.

Abstract: In one embodiment, a phacoemulsification apparatus includes actuators configured to vibrate responsively to respective driving signals, a needle including an aspiration channel, and configured to be vibrated by the actuators so as to emulsify a lens of an eye, a generator configured to generate at least one of the driving signals responsively to a vibration pattern selected for the needle, the needle being configured to vibrate in accordance with the selected vibration pattern, and a sensor configured to sense a level of vacuum in the aspiration channel, wherein the generator is configured to alter at least one of the driving signals to transition vibration of the needle from a first vibration pattern selected from the group consisting of a longitudinal vibration pattern and a first helical vibration pattern, to a second vibration pattern of a second helical vibration pattern, responsively to a decrease in the sensed level of vacuum.

Abstract: Disclosed herein are novel systems and methods for synchronized streaming of electrocardiogram (ECG) signals to a display. An aspect to the invention provides for synchronizing between first and second pluralities of digitized ECG signals that are sampled from a plurality of medical devices by first and second non-synchronized utilities. One of the pluralities of analog ECG signals, preferably a far-field ECG, is selected for reference and sampled by both the non-synchronized utilities thereby yielding respective first and second digitized reference ECG signals. The reference ECG signals are compared and the results of the comparison is used for synchronizing between the first and second pluralities of digitized ECG signals. Accordingly, the techniques of the invention facilitate concurrent synchronized streaming to a display, of a plurality of digitized ECG signals from a plurality of non-synchronized medical devices. Additional aspects and features of the invention are further disclosed herein.

Abstract: A medical probe, including a flexible insertion tube having proximal and distal ends, and a basket assembly at the distal end of the flexible insertion tube. In embodiments of the present invention, the basket assembly includes a plurality of spines and a plurality of electrodes, each of the electrodes having a lumen therethrough fitting a given spine.

Abstract: A pump device includes a rotary motor, a compartment for insertion of a disposable pump part, and one or more pulsation-reduction elements. The disposable pump part includes an input port, an output port, and a dual-action reciprocating assembly. The input port is configured for intaking fluid. The output port is configured for outputting the fluid. The dual-action reciprocating assembly is configured for pumping the fluid. The assembly includes a single piston and a rod configured to be coupled to the rotary motor, so as to drive the piston. The one or more pulsation-reduction elements are configured to reduce a pulsation in the outputted fluid, caused by the single-piston dual-action reciprocating assembly.

Abstract: A method and an apparatus configured to perform the method, the method including selecting a first maximum radiofrequency (RF) power for a first ablation mode within a range of 70 W to 100 W and selecting a second maximum RF power for a second ablation mode within a range of 20 W to 60 W. The method also includes selecting a maximum allowable temperature, of tissue to be ablated in the first ablation mode, within a range of 55° C.-65° C., and selecting irrigation rates for providing irrigation fluid to the electrode in the first ablation mode and the second ablation mode within a range of 8-45 ml/min. In some embodiments, the first maximum RF power is 90 W applied for 4 seconds with a maximum temperature of 60° C.

Abstract: In one embodiment, a medical system includes a catheter device configured to be inserted into a cardiac chamber of a living subject, and including a plurality of electrodes, at least one of the electrodes being configured to sense intracardiac electrograms (IEGMs), wireless communication circuitry configured to wirelessly receive pacing data based on at least one pacing parameter; and a signal generator configured to generate a pacing signal responsively to the received pacing data and apply the pacing signal to one of the electrodes.

Abstract: In one embodiment, a dongle apparatus configured to augment a patient interface unit (PIU) retrofitted with the dongle apparatus, and including a connector configured to be physically connected to an interface of the PIU, at least three load circuits configured to receive at least three corresponding alternating current (AC) signals from the PIU via the connector and mimic a load of at least three corresponding magnetic field generator coils of a location pad, sampling circuitry configured to sample a current amplitude and a phase of the at least three AC signals in the at least three load circuits, and wireless communication circuitry configured to wirelessly send data about the current amplitude and the phase of the at least three AC signals to a driver of the location pad. Other embodiments are described herein.

Abstract: A system includes a processor and a display. The processor is configured to: (a) receive an optical image of an organ of a patient, (b) receive an anatomical image of the organ, (c) receive, from a position tracking system (PTS), a position signal indicative of a position of a medical instrument treating the organ, (d) register the optical image and the anatomical image in a common coordinate system, and (e) estimate the position of the medical instrument in at least one of the optical image and the anatomical image. The display is configured to visualize the medical instrument overlaid on at least one of the optical image and the anatomical image.