Abstract: A method includes inserting a dilation catheter into a nostril of a patient and positioning a first dilator of the dilation catheter between a turbinate of the patient and an adjacent lateral nasal wall of the patient. The method also includes expanding the first dilator, thereby applying pressure to the turbinate of the patient, and removing the dilation catheter from the nostril of the patient.

Abstract: Planar end effector designs having irrigation are presented. The example end effectors are configured to be affixed to a distal end of a catheter and delivered through vasculature in a collapsed configuration and expand at an intracardiac treatment site to a deployed configuration. In some instances, the end effector can have an electrode array with sufficient density to perform mapping and irrigation for mapping. The end effector can include dedicated irrigation tubes and/or irrigating electrode-carrying spines to irrigate within the electrode array. Flow rate at positions within the electrode array can be controlled in a predetermined manner by varying pore/port size, flow direction, and/or flow path cross-section throughout an irrigation flow path in the end effector.

Abstract: An adapter can include circuitry that can toggle between a mapping state and an ablation state. In the mapping state the circuitry can connect the catheter to a mapping system so that the catheter can measure electrical signals from multiple independent electrodes on an end effector of the catheter. In the ablation state the circuitry can connect the catheter to an ablation generator so that the catheter can apply electrical signals to the electrodes to ablate using IRE and/or RF techniques. The circuitry can short together a group of electrodes in the ablation state and electrically isolate the electrodes in that group from each other when in the mapping state. Using the adapter, the catheter can ablate and map at a treatment site without having to be repositioned between the mapping and ablation steps.

Abstract: An apparatus includes a catheter shaft assembly and an end effector. The catheter shaft assembly includes an outer sheath with a distal end. The end effector is associated with a distal end of the catheter shaft assembly. The end effector includes a plurality of leaflets. The leaflets are configured to transition between a first configuration and a second configuration. The leaflets are configured to fit within the outer sheath in the first configuration. The leaflets are configured to expand outwardly away from the longitudinal axis in the second configuration in response to being exposed distally relative to the distal end of the outer sheath. Each leaflet includes a flexible body and a plurality of electrodes. Each flexible body defines a plurality of openings. The electrodes are positioned on the flexible body.

Abstract: An irrigation balloon catheter includes one or more inner balloons inside of an irrigation balloon. The inner balloon(s) can be compliant with a volume that is dynamically adjustable for rapid inflation, rapid deflation, complete deflation, and/or irrigation flow adjustment. An inflator tool can be configured to inflate or deflate the inner balloon to adjust flow from the outer, irrigation balloon to affect temperature at electrodes of the irrigation balloon.

Abstract: An ENT surgical instrument includes a shaft assembly, a flexible substrate, and at least at least one electrically-conductive sensor trace formed on the flexible substrate. The shaft assembly has a distal end sized and configured to fit in an anatomical passageway in an ear, nose, or throat of a patient. The flexible substrate extends along at least a portion of the shaft. The at least one sensor trace includes at least one concentric loop portion, wherein the at least one concentric loop portion defines at least one navigation sensor.

Abstract: An irrigation balloon catheter includes one or more inner balloons inside of an irrigation balloon. The inner balloon(s) can be compliant with a volume that is dynamically adjustable for rapid inflation, rapid deflation, complete deflation, and/or irrigation flow adjustment.

Abstract: A control handle for a steerable catheter allows for precise manipulation of the distal catheter tip in a target organ or vessel using only one hand. The control handle can have a single articulating knob capable of both linear translation along and rotation about the axis of the handle. These functions of the articulating knob actuate both the expansion and retraction of an expandable member, as well as bi-directional deflection of the distal catheter tip. The articulating knob functions with consistency regardless of the orientation of the handle, with ergonomic movements allowing the user to comfortably keep their attention on the procedure's monitoring equipment. These improvements can lead to safe and more rapid procedure times for procedures such as diagnostics and cardiac ablation.

Abstract: A catheter system to record and map electrical signals by cardiac tissues before, during, and/or after the treatment of cardiac arrhythmias in a group of patients. The system can include an elongated body; a distal electrode assembly comprising a proximal stem, a plurality of spines emanating from the stem; and a plurality of nonconductive spine covers, each surrounding a respective spine. Each spine can cover one or more tensile members of the respective spine cover. The system can be configured to achieve clinically improved performance and safety of catheter configurations as to accessibility into target areas of a beating heart.

Abstract: A catheter system to record and map electrical signals by cardiac tissues before, during, and/or after the treatment of cardiac arrhythmias in a group of patients. The system can include an elongated body; a distal electrode assembly comprising a proximal stem, a plurality of spines emanating from the stem; and a plurality of nonconductive spine covers, each surrounding a respective spine. Each spine can cover one or more tensile members of the respective spine cover. The system can be configured to achieve clinically improved performance and safety of catheter configurations as to accessibility into target areas of a beating heart.

Abstract: Examples presented herein generally include systems and methods which can contact electrodes to cardiac tissue while sensing electrical potential from fluids near the tissue. The electrodes in contact with the tissue can be carried by an end effector and can be used to sense and/or ablate the tissue they contact. A reference electrode can be insulated by a shaft connected to the end effector so that the reference electrode can sense the electrical potentials from the fluids near the tissue while being prevented, by the shaft geometry, from contacting the cardiac tissue. In some examples, the reference electrode can be tubular, having an inner surface that is configured to contact and sense electrical potentials from the fluids and an electrically insulated outer surface. Configured as such, the reference electrode can serve as an extension of an irrigation tube extending through the shaft.

Abstract: An apparatus includes an end effector having loop members with electrodes thereon and is usable with catheter-based systems to measure or provide electrical signals. The end effector can include three loop members that are non-coplanar when expanded unconstrained that become contiguous to a planar surface when the loop members are deflected against the surface, a mechanical linkage that joins the loop members at a distal vertex of the end effector, electrodes having surface treatment to enhance surface roughness of the electrodes, twisted pair electrode wires, a bonded spine cover, and/or any combination thereof.

Abstract: A catheter system to record and map electrical signals by cardiac tissues before, during, and/or after the treatment of cardiac arrhythmias in a group of patients. The system can include an elongated body; a distal electrode assembly comprising a proximal stem, a plurality of spines emanating from the stem; and a plurality of nonconductive spine covers, each surrounding a respective spine. Each spine can cover one or more tensile members of the respective spine cover. The system can be configured to achieve clinically improved performance and safety of catheter configurations as to accessibility into target areas of a beating heart.

Abstract: An electrophysiology catheter with a distal electrode assembly having covered spine carrying a plurality of microelectrodes. One or more spines have preformed configurations including at least a first portion with a first curvature and a second portion with a second curvature, and may include a linear portion. The linear portion may be between the first and second portions. The linear portion may be distal of the first and second portions. One or more spines have a narrower portion so that different portions of the spine can have different flexibility with a degree of independence in flexibility from adjacent portions.

Abstract: An electrophysiology catheter with a distal electrode assembly having covered spine carrying a plurality of microelectrodes. The spines have nonconductive covers that are reinforced with tensile members, e.g., wires or fibers, that extend (or have portions that extend) longitudinally so as to minimize any elongation of the covers and the microelectrodes carried thereon. The tensile members may also have a length greater than the length of the spines so the proximal portions extend proximally from the spines, through the catheter and at least into the control handle for actuation by an operator for deflecting and moving the spines, like “fingers.

Abstract: An apparatus includes a catheter body and an end effector. The catheter body has a distal end and is sized and configured to fit within regions of a cardiovascular system. The end effector is at the distal end of the catheter body and is sized and configured to fit within regions of a cardiovascular system. The end effector includes an end effector body, an electrode, and a sensor. The end effector body has an outer surface. The electrode has a tissue contact surface. The sensor has a tissue contact surface. The sensor is configured to sense at least one condition associated with tissue contacting the tissue contact surface of the sensor. The tissue contact surface of the sensor is configured to protrude relative to one or both of the outer surface of the end effector body member or the tissue contact surface of the electrode.

Abstract: An electrophysiology catheter with a distal electrode assembly having covered spine carrying a plurality of microelectrodes. One or more spines have preformed configurations including at least a first portion with a first curvature and a second portion with a second curvature, and may include a linear portion. The linear portion may be between the first and second portions. The linear portion may be distal of the first and second portions. One or more spines have a narrower portion so that different portions of the spine can have different flexibility with a degree of independence in flexibility from adjacent portions.

Abstract: A catheter includes a catheter body and a distal tip section that includes an elongated member that extends along a longitudinal axis. An anchor mechanism can be disposed along an outer surface of the elongated member and/or within the elongated member in a first configuration. In a second configuration, the anchor mechanism can be configured to extend radially outward with respect to the longitudinal axis to surround at least a portion of the distal tip section.

Abstract: A method is used to manufacture a surgical instrument. The surgical instrument includes a catheter and an end effector extending distally from the catheter. The method includes forming at least one electrode, sensor, or thermocouple onto the catheter or the end effector of the surgical instrument by etching or vapor depositing a three-dimensional structure onto a non-conductive material that is layered over a super elastic material.

Abstract: An apparatus includes a catheter shaft assembly and an end effector. The end effector includes a plurality of strips and a plurality of electrodes. The strips are configured to fit within an outer sheath of the catheter shaft assembly in a first configuration. The strips are configured to expand outwardly away from a longitudinal axis defined by the catheter shaft assembly in a second configuration when exposed distally relative to the distal end of the outer sheath. The electrodes are positioned on at least some of the strips. The electrodes are positioned relative to each other such that groups of four of the electrodes define a substantially square configuration.